GLOBALG.A.P. IT Platform

Find answers to frequently asked questions regarding the new GLOBALG.A.P. IT platform.
Generic selectors
Exact matches only
Search in title
Search in content
Post Type Selectors

Browse by topic

General questions
Audit
Work order
Certificate
Migration
Site/PHU/Product
Roles
Upload sheet
API
Add-ons
Benchmarked schemes
Training
Mobile solution
Language availability
Invoicing
Certification cycle alignments in CertifierOS

This article applies to the following Farm Assurance Products whose valid-to dates need to be aligned with the main standard (IFA): GRASP,  FSMA, AH-DLL GROW and NURTURE.

It also applies to QS-GAP alignments with the QS Database and QS FIAS alignments with the main standard QS-GAP.

If you need to adjust the valid-to date, you have two options:

  1. Align it during the next audit or assessment, or
  2. Initiate a modification audit to update the valid-to date immediately following the launch of CertifierOS on 03/11/25.

To proceed with the modification audit, you must first create the producer’s site(s) and product(s).
If the alignment shall be done for a Producer Group (PG), this includes creating the sites and products for all PG members.

See here how to create a site.

See here how to create a product and add it to a site.

Note: Creating sites and their associated products is a one-time setup. This process does not need to be repeated for future audits or assessments.

To create the modification audit/assessment work order you need to select "+ Create" from the audit section in CertifierOS:

Select the applicable Farm Assurance Product and properly name the audit/assessment: and click continue:

In this random example we select a GRASP v2 assessment:

Select the producer and the contact person and click continue:

Now we need to select the

"Reporting option" (in this random example it is an option 1 single site)

The "Organization" (your CB)

Under "Audit type" we need to select "Modification audit"

Under "Audit Peoduct Category" we select the appropriate option. Note that only for GRASP "Non-applicable" is the correct option. For other FAPs, it can be F&V, F&O, AQ, etc.

Please also note that the "GRASP V2 - Checklist type" shall only be selected in case of a GRASP assessment. For all other FAPs this field shall remain empty:

We select the audit address and submit the work order:

With this we have created our modification scope work order. Now we have to select the "Products" tab:

And add the products to the certification/assessment scope

We click on "Advanced Search":

First click on the siphon icon, -> select "Product" -> Apply -> select the applicable product(s) -> click "Add":

Click Save:

With this, the system triggers the appropriate smartforms, which can be found under the checklist tab. The smart forms have to be filled out as explained in this recording. Please not you can also user the Attribute mass entry feature.

After the smart forms are filled out you need to close the smart form as closed compliant:

The next step is to issue the new version of the certificate/Letter of conformance via the certification section. Click on "+ New Certificate:

Under "Audit" select the audit/assessement you have just finalised, under "Status" depending on the FAP, either Certified or Assessed and under "Certificate Document Template" the applicable template. (Find here the instructions how to create your CB's certificate templates). You select the validity dates to align with the main certificate and click on "Generate"

Documenting species of Flowers & Ornamentals in CertifierOS

CBs can record product-specific varieties in the product attribute smart forms for all products, including Flowers and Ornamentals:

However, due to technical limitations, this information cannot be displayed on the certificate.

How to find the latest wiki articles?

Find here the link to the landing page of the new IT platform wikis:

https://ggwiki-globalgap.org/it-platform/

This is the view you will see:

When you select a topic—such as "audit" in this example—the most recent wikis related to that topic will appear below. These wikis are displayed in order from newest to oldest.

When you reach the bottom of the page, you can click on "View all" to access all articles or this section:

The articles in this section are also presented in descending order by publication date, with the most recent appearing first:

How to find audits/work orders in CertifierOS

CertifierOS allows the search via the top left-hand side search field and the "Filter" button on the top right-hand side.

The left-hand side search can be used to search via "Audit IDs", a full-text search or a partial text search, e.g. the GGN or part of the audit/work order title.

It is suggested to use the "Filter" search where you can filter out e.g. via the producers name or ggn. Please press on 'Apply' to activate the search:

How to navigate in CertifierOS

After logging in to CertifierOS, you will be redirected to the Home page. From the bottom left side, you can expand the left-hand side navigation bar:

Via this navigation bar and clicking on the expansion arrows on its right-hand side, you can directly access:

Audits, Tickets (NCs), the Scheduler, Products/Sites/PHUs, Producers, your users, devices, certificates and the advanced configurations for creating certificate templates.

Note: Your view will display less information than the screenshot below, as the screenshot reflects the administrator's perspective:

If your user is associated with more than one CB, you can choose the appropriate one for each audit by clicking the button in the top left corner and selecting the desired CB using the checkboxes.

By clicking on your name abbreviation at the top right-hand side, you can directly access your profile settings, view the current software version you are working with, and access the Supply Chain Portal (Switch solution).

Under 'Audits', and depending on your user's access rights, you will see all audits (work orders) that have been created by your CB, or those you have created or been assigned to. By clicking "+ Create" you can start a new audit/work order:

Under 'Tickets' and depending on your user's access rights, you will see all tickets (NCs) that have been created by your CB, or those you have created or been assigned to. By clicking "+ Create" you can start a ticket/NC:

Under 'Scheduler', you can assign audits to an auditor who has installed the mobile app on their mobile device based on these instructions:

Under 'Product/Sites/PHU Browser' and depending on your user's access rights, you will see the sites (Production sites, PHUs and PG/multisite scope information sites) and products registered to these sites that have been created by your CB. By clicking "+ Add Product/Site/PHU", you can create new assets:

Under 'Producers' and depending on your user's access rights, you will see your CB's Producers. By clicking '+ Add Producers', you can create new ones:

Under 'Administration -> Users' and depending on your access rights, you may see either all or your own user. By clicking on '+ Create user', the SM can create new ones, and by clicking on the three dots at the right-hand side, you can access the profile of each user.

Under 'Administration -> Devices' and depending on your access rights, you may see either all or your own user's mobile device license key information. By clicking on 'Create single license', you can create new licenses based on these instructions.

Under 'Certificates' and depending on your access rights, you can see the certificates issued by your CB. You can search by producer GGN and name, and by clicking '+ New Certificate', you can issue a new certificate based on a successfully completed audit/assessment. By clicking on the three dots on the right-hand side you can amend a certificate, e.g. extend it.

Under 'Advanced configurations -> Global -> Document templates', you can create your CB's certificate templates based on these instructions.

Note: Please disregard any buttons not covered in this article.

Mobile App Onboarding Instructions for iOS Devices (iPhones & iPads. Mac books are not supported)

Prerequisite: The user has a license key available and a user in the CertifierOS portal
Note: Depending on the device and software version, the user experience may differ
from the one described below

PREPROD Environment

  1. Install the mobile application for testing in PREPROD environment. The
    application is available in the App Store: osapiens HUB for Service PP in
    App Store

    a. Note that the application needs to be installed directly on the device
    where the application is intended to be used
  2. Once the application has been installed, open the application
  3. Enter the license key and select “Activate Device”
  4. In the next screen, select “Synchronize” so that organizational settings of your
    CB are imported
  5. Enter the username and password of the user who will use the mobile
    application. The username and password are the same that are used to log in to
    the online portal for Certifier OS
  6. The user should now see the audit overview screen and the different audits that
    have been assigned to the user

LIVE Environment

  1. Install the mobile application for use in the LIVE environment. The application is
    available in the App Store: osapiens HUB for Service in App Store
    a. Note that the application needs to be installed directly on the device
    where the application is intended to be used
  2. Once the application has been installed, open the application
  3. Enter the license key and select “Activate Device”
  4. In the next screen, select “Synchronize” so that organizational settings of your
    CB are imported
  5. Enter the username and password of the user who will use the mobile
    application. The username and password are the same that are used to log in to
    the online portal for Certifier OS
  6. The user should now see the audit overview screen and the different audits that
    have been assigned to the user
If an option 1 producer has e.g., IFA, GRASP and SPRING  - do we have to create 3 work orders? And do we have to create the sites and their products for each standard separately?

In this case, three distinct work orders must be created-one each for IFA, GRASP and SPRING. The process begins with the creation of the IFA work order, from which the GRASP and SPRING add-on work orders will be subsequently generated and linked.

Please note that the sites and their products must be created only once for the producer and can be used for all applicable Farm Assurance Products, and also for all future audits/assessments.

Is the creation of a site (and PHU in case of product handling) obligatory for every producer also for benchmarked schemes?

Yes, all sites and PHUs (if applicable) and their respective products need to be created.

How can I add a new producer group member that does not own a GGN to a PG?

First, you need to create a producer, her/his sites and products as seen in the recordings.

Next step is to add the newly created producer to the PG as seen here at minute 1:49.

Should the audit scope of an option 2 cover all Producer group members/products/PHUs or only sampled items?

Everything that needs to be listed on the certificate must be included in the Certification scope work order of the Option 2.

This includes all producer group members, PG's own fields (if applicable), all PHUs (central, external, and member), and all products.

How to Amend Work Orders When Audit Findings Require Changes


If an auditor discovers missing information during an audit (like an undeclared PHU or crop that wasn't mentioned in the initial application), the work order must be replaced.

To make these changes, you'll need an internet connection. Add all information, including the new information, e.g. in this scenario, create the PHU entries and their products. Once everything is updated, start a new audit using the corrected information.

The same applies also in the case of a GRASP assessment other conditions apply compared to the application (e.g. a family farm was expected, but hired workers are present at the farm)

Please note that the aforementioned actions cannot be performed via the mobile app.

CertifierOS Terminology

This wiki contains only the terms that have been newly introduced in the new GLOBALG.A.P. IT system platform.

  • External ID:

For the time being CertifierOS (CoS) is using the term "External ID" instead of the GGN or GLN. This will be amended in the future:

  • D-U-N-S Number

A "D-U-N-S Number" is an identification number similar to the GS1 system, and if available, it can be added to the producer's master data voluntarily.

The term "Organization" is used for "Certification body"

  • PG/multisite scope information (Site):

This is a "dummy" site/parent entity category that the system requires to introduce the PG's/Option 1 multisite with QMS scope into the certificate.

All the PG's/Option 1 multisite with QMS products need to be added to this "dummy" site.

  • Central PHU

"Central PHU" shall be used for the PHUs operating under the QMS of an Option 2.

  • Parent:

It is an item that has a hierarchy over another item.

E.g., a production site is a parent to a product that is produced on that side.

When creating a product, this is added to the "Parent". In this context, the "Parent" is the site where this product is produced.

A PG is a parent to a Producer Group Member.

When adding a producer group member to a PG, the PG is considered a "Parent" and the producer group member a "Child":

  • Sub Producer:

A Sub producer is a Producer Group Member

  • Work order:

A work order can be an audit report or the working file where the certification scope of a legal entity is managed. A work order contains one to several smart forms that define the contents and the purpose of the work order.

A work order is either a full or a part of an audit. Meaning it can be the complete audit for an option 1, or it can be, e.g., only the Certification Scope Management work order, or the QMS audit for a PG or a producer member audit/assessment.

  • Smart form:

Smart forms are checklists which contain either attribute questions or P&Cs.

  • Option 2 - Certification Scope Management work order:

For an option 2 certification, the system requires a central work order, which is called "Certification Scope Management" work order.

In this work order, the complete certification scope information for an Option 2 is collected and needs to include:

- PG’s certification scope

- Producer Group Members

- their product scope

- Producer group members' PHUs and their product scope (If applicable)

- PG’s Central PHU(s) and their product scope(s) (If applicable)

Please note that a certification can only be created from a single work order and not from a combination of several work orders. Therefore, the "Certification Scope Management" work order of an Option 2 will have to include all the information that is needed for the specific certificate.

The certification scope management work order is the basis of every PG audit, and it shall be the starting point for the creation of all work orders that are required to complete the audit:

- The QMS audit and

- the producer group member sample audits

  • Option 1 - Certification Scope Management multisite with QMS and Option 3 - Certification Scope Management multisite with QMS

In these work orders, the complete certification scope information for an option 2 multisite is collected and needs to include the information for the option 1, all its sites and PHU(s) (if applicable).

  • "Certification Scope Management" work order audit type:

This audit type is required for a) Option 2 - Certification Scope Management, b) Option 1 - Certification Scope Management multisite with QMS and c) Option 3 - Certification Scope Management multisite with QMS work orders. See example for a):

  • Scheduler:

The CoS functionality that allows the CB to assign audits/work orders to the mobile app of an auditor:

How to search for a PG member in the Supply Chain Portal?

You can search for the producer group members inside the group´s certificate by GGN and by the producer´s name using this search bar:

How to assign an audit to an auditor

In case the audit is programmed to be audited via the mobile app, you can drag and drop the audit work order(s) to the selected auditor via the Scheduler section in the web portal.

Via "Search by name" and "Search for Audit ID or Title, you can easily filter out the auditor and work orders.

Please note that you can drag and drop by clicking on the 6 dots right next to the audit ID. Once an audit work order is assigned, the six dots are no longer visible.

Once the audit work order is assigned to the auditor, click on it to activate it. Then, select "Release Selected" to send the audit to the auditor's mobile app. You’ll notice the audit work order changes to a darker colour, indicating it has been successfully released.

If needed, you can withdraw the audit work order from the auditor by right-clicking and selecting "Delete".


For assigning work orders to the mobile app, find additional information here.

To assign the audit work order via the portal, press the two people icon on your right-hand side:

Press on "Add member"

Select the applicable role by pressing on the first field of the pop-up window:

Select the applicable person from the second field:

You can filter out the applicable person by typing her/his name.

Where can I find the traning material for the new GLOBALG.A.P. IT platform?

You can find here the recordings for the CertifierOS

You can find here the information regarding the Mobile application (for offline use)

You can find here the information regarding the bulk upload tool

You can find here the recordings for the Supply Chain Portal

View all
Certification cycle alignments in CertifierOS

This article applies to the following Farm Assurance Products whose valid-to dates need to be aligned with the main standard (IFA): GRASP,  FSMA, AH-DLL GROW and NURTURE.

It also applies to QS-GAP alignments with the QS Database and QS FIAS alignments with the main standard QS-GAP.

If you need to adjust the valid-to date, you have two options:

  1. Align it during the next audit or assessment, or
  2. Initiate a modification audit to update the valid-to date immediately following the launch of CertifierOS on 03/11/25.

To proceed with the modification audit, you must first create the producer’s site(s) and product(s).
If the alignment shall be done for a Producer Group (PG), this includes creating the sites and products for all PG members.

See here how to create a site.

See here how to create a product and add it to a site.

Note: Creating sites and their associated products is a one-time setup. This process does not need to be repeated for future audits or assessments.

To create the modification audit/assessment work order you need to select "+ Create" from the audit section in CertifierOS:

Select the applicable Farm Assurance Product and properly name the audit/assessment: and click continue:

In this random example we select a GRASP v2 assessment:

Select the producer and the contact person and click continue:

Now we need to select the

"Reporting option" (in this random example it is an option 1 single site)

The "Organization" (your CB)

Under "Audit type" we need to select "Modification audit"

Under "Audit Peoduct Category" we select the appropriate option. Note that only for GRASP "Non-applicable" is the correct option. For other FAPs, it can be F&V, F&O, AQ, etc.

Please also note that the "GRASP V2 - Checklist type" shall only be selected in case of a GRASP assessment. For all other FAPs this field shall remain empty:

We select the audit address and submit the work order:

With this we have created our modification scope work order. Now we have to select the "Products" tab:

And add the products to the certification/assessment scope

We click on "Advanced Search":

First click on the siphon icon, -> select "Product" -> Apply -> select the applicable product(s) -> click "Add":

Click Save:

With this, the system triggers the appropriate smartforms, which can be found under the checklist tab. The smart forms have to be filled out as explained in this recording. Please not you can also user the Attribute mass entry feature.

After the smart forms are filled out you need to close the smart form as closed compliant:

The next step is to issue the new version of the certificate/Letter of conformance via the certification section. Click on "+ New Certificate:

Under "Audit" select the audit/assessement you have just finalised, under "Status" depending on the FAP, either Certified or Assessed and under "Certificate Document Template" the applicable template. (Find here the instructions how to create your CB's certificate templates). You select the validity dates to align with the main certificate and click on "Generate"

How to find audits/work orders in CertifierOS

CertifierOS allows the search via the top left-hand side search field and the "Filter" button on the top right-hand side.

The left-hand side search can be used to search via "Audit IDs", a full-text search or a partial text search, e.g. the GGN or part of the audit/work order title.

It is suggested to use the "Filter" search where you can filter out e.g. via the producers name or ggn. Please press on 'Apply' to activate the search:

How to link existing audits in CertifierOS

To associate existing audits or work orders—such as a GRASP assessment—with an IFA audit, please access the audit you regard as the primary one. Then, select the connector icon located in the upper right-hand corner of the interface.

Note: To connect work orders, the primary work order must be in status "Open":

Next, select “Add Link” followed by “Add Existing Item” to proceed with the association:

Within the pop-up window, please select the “Related To” option to define the connection:

From the magnifier icon, select “Audits” to specify the type of item to be linked:

By clicking on the search field, a list of all work orders issued by your CB will be displayed. You may scroll through the list to locate the relevant item, or alternatively...

You may search either by the work order number or by the work order name to locate the desired item more efficiently.

To select the appropriate work order, click on its status as indicated below.

Please note that if you click on the URL instead, you will be redirected to the work order itself rather than establishing a link between the items.

Finally, click on “Add Link” to complete the association between the selected items:

With this action, the two work orders have been successfully linked:

How to create a GRASP assessement work order in CertifierOS

You can start preparing the GRASP work order either directly by clicking on "+ Create" or by linking it from an existing IFA work order.

To see how to create a GRASP work order from an existing IFA audit work order, please see this recording.

In this example, we will start the process by clicking on "+ Create".

In the pop-up window, select "GRASP V2" and assign an appropriate name to the assessment, following the example shown below:

As always, we select the producer and the contact person:

On the next pop-up window page, we will have to select:

The Reporting option, according to the situation. Here we selected an Option 1 - Single Site Certification

Our CB under "Organization"

The "Audit type", according to the applicable audit type. In this example, we selected "Initial certification audit"

The "Audit Product Category". In GRASP assessment work orders, we need to select "Non-applicable"

The "GRASP v2 - Checklist type" depending on the worker's situation on site. See the available options below. In this example, we selected "GRASP v2 - Hired/Subcontracted workers (Initial year)"

Please ensure that the field 'GRASP v2 - Checklist type' is used exclusively for GRASP work orders. If applied to other types of work orders, such as IFA, it will cause the system to trigger incorrect smart forms.

As always, we select the audit address and submit:

With this step, the GRASP assessment work order has been successfully created. The next action is to include the relevant product(s) within the assessment scope, as we do for any other Farm Assurance Product. We select the "Products" tab:

and click on "Add Product/Site/PHU"

In this example, the product is "Maria Carrot's (6291041011566) product carrot"

With this, the applicable smart forms for our assessment were triggered and can be seen in the relevant tab:

The remaining process is identical to any other Farm Assurance Product.

How to use the smart form attribute mass entry feature in CertifierOS

Once the audit work order has been created and the relevant products have been added to the scope, proceed by selecting the Checklist tab (Checklisten).

From the left-hand side, you can choose the smart forms you want to work with. To activate all smart forms at once, click the first checkbox; however, it is recommended to select only the attribute-specific smart forms.

Once you've selected at least one smart form, the "Answer Shared Questions" button on the right-hand side will become active:

Clicking it will open the following pop-up window.

On the left-hand side, you'll find a list of all questions that appear in more than one smart form. You can scroll vertically to browse through them and select any question directly. At the top, there's a search field that enables you to filter and locate specific questions quickly.

On the top right, the currently active question is displayed. Just below it, you'll see the corresponding answer field, which may either be a predefined selection or a free-text input:

For any questions where it is appropriate, you can respond to all smart forms at once by enabling them simultaneously. Via the first tick box you can enable all smart forms at once:

Or by using the filters "Checklists", "Product asset name", "Product" and "Producer". In this example, we selected a producer:

Note: To deactivate a filter, simply click on your current selection again.
In the example above, you would need to click on "Tony Mango" to remove the filter.

To correctly answer and save a question, follow these steps:

  1. Provide your answer to the question
  2. Select the relevant smart forms (you can choose one or multiple)
  3. Click the blue "Apply selected" button
  4. Click the blue "Confirm and Next" button

Important: If you do not press "Confirm and Next", your answer will not be saved:

After answering the final question and clicking "Confirm," the pop-up window will close, and you'll be redirected to the smart form overview page. Each smart form should then be reviewed and closed as usual.
Reminder: It is recommended to use "Save and Submit" only after the audit review has been completed.

Important: Please note that the order of the questions displayed on the left-hand side is currently incorrect. For example, related items such as "999001 Non-Covered Crops First Harvest in hectares" and "999100.01 Number of growing cycles for covered crops - Number" are not listed consecutively. We are aware of this issue and are actively working to resolve it.

Note: You can still choose to complete the smart forms individually, one at a time.

How to create a Compound Feed Manufacturing (CFM) v3.1 audit in CertifierOS

To start a GLOBALG.A.P. Compound Feed Manufacturing v3.1 audit, we need to create our certification scope. To do so, we first must create the producer’s product scope site. We start by selecting the Type “Sites/PHU” and afterwards one of the applicable "Sites/PHU and Category "GLOBALG.A.P. Compound Feed Manufacturing - Scope Registration (Site)":

As per standard practice, proper site naming is essential:

As always, we select the producer. In this example, it is the producer “CFM Test Producer”:

Please note that adding a contact person is not required.

We do not add a Parent; we select our CB under organization and submit. As always, you can add tags or a description to the respective fields. Please note that for the scope site, an address is not required:

The next step is to add the certification scope (product) to the site above.

The available products for this FAP are:

“Compound Feed for Aquaculture” (ID: 10949) &

“Compound Feed for Livestock” (ID: 10950)

As always, we select Type “Product” and properly name it. In our example, the certification scope is “Compound Feed for Aquaculture”:

We select the producer:

In our example, we will select the product “Compound Feed for Aquaculture” (ID: 10960), select under Parent the site we have created before, add our CB under Organization and press on submit:

We select the parent and submit:

Note: This standard does not require a PHU.

To summarise, in our example, we have created,

  • A CFM scope site,
  • Added product “Compound Feed for Aquaculture” to the scope site.

Please note that the creation of the scope site and product scope needs to be done only for the first audit and can be used for all future audits.

After having finalised the creation of the scope, we can start the audit in the same way as always by selecting the Farm Assurance Product (FAP). First, we select the relevant FAP and the applicable reporting option:

 In our scenario, we select Option 1 - Single Site Certification. Proper audit naming is essential:

We select the producer and contact person:

We select our CB, and under Audit type, we select the applicable option. In our example, we selected “Initial certification audit”.

Note: for all GLOBALG.A.P. Compound Feed Manufacturing v3.1 audits, under Audit Product Category, we shall select “GLOBALG.A.P. Compound Feed Manufacturing scope”:

We click through the pop-up window by clicking “Continue” and “Submit” the audit.

The next step is to add the Scope information to our audit:

&

With this, the proper smart forms will be triggered:

Please note that during the creation of this wiki, the P&C smart form was not available. This is the reason it is not displayed in the above screenshot.

After filling out the smart forms and finalizing the audit, the certificate can be issued as explained in this wiki.

How to create a GLOBALG.A.P. NON-GM/Ohne Gentechnik Add-on audit in CertiferOS

To initiate a GLOBALG.A.P. Non-GM/Ohne Gentechnik Add-on audit, we need to define our certification scope. To do so, we first must create the producer’s product scope site. We start by selecting the Type “Sites/PHU” and afterwards one of the applicable “NON-GM/Ohne Gentechnik Add-on” scope sites:

As per standard practice, proper site naming is essential:

As always, we select the producer. In this example, it is the producer “Non GM test producer”:

Please note that adding a contact person is not required.

We do not add a Parent; we select our CB under organization and submit. As always, you can add tags or a description to the respective fields. Please note that for the scope site, an address is not required:

The next step is to add the certification scope (product) to the site above. As always, we select Type “Product” and properly name it. In our example, the certification scope is “CFM for Livestock”:

We select the producer:

Under product type, for the FAP GLOBALG.A.P. NON-GM/Ohne Gentechnik Add-on, we have the following product options:

  • CFM for Livestock (ID: 10945)
  • CFM for Aquaculture (ID: 10946)
  • IFA for Aquaculture (ID: 10647)
  • CoC for Aquaculture (ID: 10948)

In our example, we will select the product “CFM for Livestock”, select under Parent the site we have created before, add our CB under Organization and press on submit:

In case the producer operates a PHU, we shall create one in the same way as for IFA. Proper naming is essential:

The next step is to add the product to the PHU we have just created:

As always, we select the producer and contact person:

At the next step, we need to select the product “CFM for Livestock” and select the PHU:

To summarise, in our example, we have created,

  • A Non-GM scope site,
  • Added product “CFM for Livestock” to the scope site.
  • A Non-GM scope PHU,
  • Added product “CFM for Livestock” to the scope PHU.

Note: The creation of the scope site and product scope needs to be done only for the first audit and can be used for all future audits.

After having finalised the creation of the scope, we can start the audit in the same way as always by selecting the Farm Assurance Product (FAP). First, we select the relevant FAP:

In our example, we selected Module 1 and as the reporting option “Option 1 - Single Site Certification” and named the audit:

 As always, we select the applicable producer:

Under Audit type, we select the applicable option. In our example, we selected “Initial certification audit”.

Please note that for all Non-GM modules under the Audit Product Category, we shall select “GLOBALG.A.P. NON-GM/Ohne Gentechnik scope”:

We click through the pop-up window by clicking “Continue” and "Submit" the audit.

The next step is to add the Scope information to our audit:

In our example, we are selecting the product we had previously named “Non GM test producer product scope CFM for Livestock”:

With this, the proper smart forms will be triggered:

After filling out the smart forms and finalizing the audit, the Letter of Conformance can be issued as explained in this wiki.

Note: in case the certification scope for GLOBALG.A.P. NON-GM/Ohne Gentechnik Add-on is “IFA for Aquaculture” and the producer is an Option 1 – Multiside with QMS, when creating the scope site, the option “GLOBALG.A.P. NON-GM/Ohne Gentechnik Add-on - Scope Registration QMS (Site)” must be selected:

Note:
The available certification options per module for this Add-on can be seen below:

How to issue a certificate/Letter of conformance in CertifierOS?

After the audit/assessment is successfully finalised and the audit work order is closed as "Closed compliant",

we can issue the certificate/Letter of Compliance (LoC). To do so, we need to go to the certificate section and press on "+ New Certificate":

After clicking on the "Audit" field, in the pop-up window, we can select the applicable audit. Please note that here, all your CB's closed-compliant audits/assessments will be listed.

By clicking on the "Status" field, you can select the applicable status.

Please note that in case a certificate needs to be issued, the status "Certified" must be selected. In case a Letter of Conformance has to be issued, the status "Assessed" has to be selected.

The next step is to select the applicable certificate template by pressing into the relevant field:

In our example, we have selected "IFA v6 Plant - Option 1"

The next step is to select the validity dates and press "Generate"

How to audit Chain of Custody (CoC) in CertifierOS

To start a CoC audit, we need to create our certification scope. To do so, we first must create the producer’s product scope site. We start by selecting the Type “Sites/PHU”

Then we choose the category “CoC Scope Registration (Site)”:

Next step, as always, is to properly name the site. See here an example:

The next step is to select the producer:

Please note that the CoC Scope Registration (Site) does not require an address, as its purpose is solely to record the CoC certification scope.

After we finalise the site creation process, we proceed with adding the product(s).

We select under Type “Products”, we do not choose a Category and properly name the product. In this example, we will use “Plants”:

We select the producer:

The next step is to select the product.
Please note that the only products applicable for the Chain of Custody scope are:
Plants” (ID: 10940)

Aquaculture” (ID: 10941)

Compound Feed” (ID: 10942).

 In this example, we have selected plants:

As always, for a product, we need to select under "Parent" the respective site and CB:

In case this CoC producer is also handling Aquaculture and/or Compound feed, these products must be added to the “CoC Scope Registration (Site)” in the same way as seen above.

In case the CoC producer is operating a PHU or using an external PHU, we must create them accordingly by using the highlighted options below:

After the CoC PHU/External PHU is created, we proceed with adding the product.

For a PHU, we need to select the product “CoC PHU” (ID: 10943), and for an external PHU, we need to choose the product “CoC External PHU” (ID: 10944).

In this example, we select under Product “CoC PHU” and under "Parent" the respective PHU we just created:

To summarise, in our example, we have created,

  • a CoC scope site,
  • added product “plants” to the CoC scope site,
  • created a CoC PHU site,
  • added the product “CoC PHU” to the CoC PHU site:

Please note that the creation of the scope site and product scope needs to be done only for the first audit. For all future audits, the above process shall not be repeated, as the site and product can be reused.

After having finalised the creation of the scope and, if applicable, PHU/External PHUs and their respective product(s), we can start the audit in the same way as always by selecting the Farm Assurance Product (FAP).

For CoC audits, the following options are available:

Please note that for “GLOBALG.A.P. Chain of Custody (CoC) v6.1” the available scopes are "Plants", "Aquaculture" and "Compound Feed".

For “GLOBALG.A.P. Chain of Custody (CoC) v6.1 through BRCGS”, the available scope is "Plants".

 For “GLOBALG.A.P. Chain of Custody (CoC) v6.1 through IFS”, the available scopes are "Plants" and "Aquaculture", and

for “GLOBALG.A.P. Chain of Custody (CoC) v6.1 through QS”, the available scope is "Plants".

After selecting the FAP, the certification option, naming the audit and selecting the producer in the same way as in all other audits, we need to select the applicable Audit type, Audit Product Category and Checklist type.

Under Audit Product Category, we need to select “CoC scope” and under Checklist (CL) type, only in case of GLOBALG.A.P. Chain of Custody (CoC) v6.1, we have the following two options:
- CoC-SC Supply Chain v6.1

- CoC-RSRC Retail Stores and Restaurant Chains v6.1

Please note these two CL types only apply to GLOBALG.A.P. Chain of Custody (CoC) v6.1, so they shall not be used for the other CoC FAPs.

Note: For CoC via QS/IFS/BRCGS, the Checklist type shall not be selected.

In this example, we have randomly selected the CoC-RSRC Retail Stores and Restaurant Chains v6.1 CL type.

As always, we select the producer’s product scope:

Our example producer has two products, which we will select:

With this, the necessary smart forms were triggered, which must be filled out:

Please note that P&C smart forms are only available for CoC v6.1, CoC v6.1 through QS & CoC v6.1 through IFS.

A P&C smart form is not available for CoC v6.1 through BRCGS, as the necessary information in this case is documented via the BRCGS system.

Please note that in the Certificate Data smart form, the Species documentation is mandatory for Aquaculture. In the case of Plats or Compound feed, it is voluntary. In case you do not document a specific species, please mark it as “Non-applicable”:

After all the smart forms are filled out, and in case the audit was successful, the certificate can be issued in the same way as all the other FAPs. See this wiki for detailed instructions.

How to create certificate templates in CertifierOS

CBs must upload their own certificate templates to CertifierOS for every Farm Assurance Product (FAP) they certify. Each FAP and certification option requires only one template upload.

To do so, please follow the instructions below:

The CB has to download the relevant certificate template from this GLOBALG.A.P. SharePoint folder.

See here, for example, the certificate template options available for IFA v6 SMART Plants:

Via right-click on the three dots, select 'Download' to your PC. In this example, we have chosen the template for IFA v6 SMART Plants Option 2:

After opening the template, you will see that you can only amend the highlighted parts:

Please add under <CB Logo> your CB's logo and under "<accreditation mark> No. of certification body: ${Organization.OrganizationId}" your accreditation mark, including the accreditation number. The latter shall be added only for the applicable FAPs. In case you are not yet accredited for a certain FAP, please delete the relevant icon. (After the accreditation is achieved, you can amend your template by repeating this process.)

Note: You can find the correct document version by searching the related P&Cs in the document centre. In this example, this would be the related document:

Note: The document version is not mandatory for every FAP. If the template does not include a <document version> field, the document version shall not be entered.

The final template would look like this:

Please note that for several FAPs, the templates are prepopulated.

Before proceeding to the next step, please add the signature of the authorising person.

Note: For producers and PGs that do not operate a PHU, separate templates must be used. These templates can be found in designated subfolders for each FAP, as seen in the first screenshot above.

Note: In some cases, some parts of the templates will appear corrupted, similar to the below:

This is caused by a missing font on your PC. You can find the font in this folder. Please install it on your PC to fix this issue.

Please select in CertifierOS: the gear icon at the bottom left-hand side -> Global -> Document templates:

Now select "+ Upload Template":

Name your certificate template by filling in the "ID" and "Name" fields in the pop-up. Both fields can have the same value, as demonstrated below. Please note that clear template names will allow easy access during certificate issuance. The field "ID" can be used in accordance with the CB's own procedures.

Under "Usage Context", please select "Certificate".

Under "Orzanization" select your CB.

NOTE: DO NOT switch on the "Global Template" toggle

Click on the blue "upload" field or drag and drop the template from your PC, load the document and press "Upload":

You will see that the template you just created will appear at the end of your list:

By clicking on the three dots, you can download, delete or edit your template.

If you wish to edit, you can amend the "Name" and, by clicking on the "x", you will be able to upload a new template to replace the previous one.

Please note that any template change does not affect previously issued certificates.

To use the templates, please follow the known certification process:

Select the applicable "Audit", "Status" and "Certificate Document Template". In this example, "IFA v6 SMART Plants - Option 2"

Then press "Generate":

To view the generated certificate, navigate to the Certificate section. In the 'Certificate Template' column, you can identify which certificates are already linked to a template.

Select the certificate you want to view, then click the three dots on the right side and choose 'View' from the menu:

On the next page, click on "View PDF" to download the PDF certificate.

If the certificate template needs to be updated—for example, if an incorrect template was selected or the CB logo has changed—you can do so by selecting the relevant certificate, clicking the three dots, and choosing 'Edit':

A pop-up window will appear showing the template currently in use:

Clicking on the current template field will open a drop-down menu displaying all templates created by the CB. From there, select the appropriate template and click to apply it:

Click 'Save Changes' to generate the updated certificate. You can then download it following the steps described earlier.

This is the test certificate issued based on the above process:

If an option 1 producer has e.g., IFA, GRASP and SPRING  - do we have to create 3 work orders? And do we have to create the sites and their products for each standard separately?

In this case, three distinct work orders must be created-one each for IFA, GRASP and SPRING. The process begins with the creation of the IFA work order, from which the GRASP and SPRING add-on work orders will be subsequently generated and linked.

Please note that the sites and their products must be created only once for the producer and can be used for all applicable Farm Assurance Products, and also for all future audits/assessments.

Is the creation of a site (and PHU in case of product handling) obligatory for every producer also for benchmarked schemes?

Yes, all sites and PHUs (if applicable) and their respective products need to be created.

Should the audit scope of an option 2 cover all Producer group members/products/PHUs or only sampled items?

Everything that needs to be listed on the certificate must be included in the Certification scope work order of the Option 2.

This includes all producer group members, PG's own fields (if applicable), all PHUs (central, external, and member), and all products.

How to create an option 2 audit in CertifierOS

For a new Option 2, you need to create a parent site "PG/Multisite scope information (Site)" and assign all products of this PG to this parent site:

Note: The process for adding the product(s) to the "PG/Multisite scope information (Site)" is identical to the process for creating any other product.

In case the PG operates a PHU under its QMS, you need to create a "Central PHU" and add to it any applicable product(s):

If the PG is using an external PHU, this site must also be created. The Site Category in this scenario is "External PHU".

Note: The above assets have to be created only once and can be used for all future audits.

Before you can add members to the producer group (PG), you must first create the members themselves, set up their respective sites, and create and assign their products to those sites. The producer creation is shown in this recording, and the site and product creation can be seen here and here, respectively.

After our members are created, we can add them to the PG. We go to our PG and click on "+ Add entry:

You can search for the producer group members by GGN or name. You select via the tick boxes and press "Add":

In this example, we selected two producer group members:

If the PG has its own production, she must also be added as a member, following the same procedure described above.

Once the above steps are completed, the members will appear under the PG's producer hierarchy:

Now we can start preparing the required work orders. The first work order (WO) that needs to be created is the "Option 2 - Certification scope Management" WO, as seen below. We first select the applicable FAP and properly name the audit:

We select the PG and the contact person:

As this is the Certification Scope WO, under "Reporting Option", we must select "Option 2 – Certification Scope Management". Then, under "Organization", choose your CB. For "Audit Type", select "Certification Scope Management", and under "Audit Product Category", choose the applicable option(s) and click on Continue. In this example, we’ve selected Fruit & Vegetable, as shown below:

We select the audit address and click on Submit:

With this, we have created our certification scope work order. Now we have to add our producer group members and products by clicking on the respective tabs:

To add the members, we click on "Add New":

Select the producer by searching using their name, GGN, or the Advanced Search. Once all members have been selected, click "Save". Please also ensure that the PG is added as a member if it has its own production:

In the next step, we need to add the product by selecting the respective tab and clicking on "Add Products/Site/PHU:

It is advised to select the "Advanced search":

To include products in the scope, follow these steps:

Click the siphon icon.
Select the Type as "Product".
Ensure that all PG members, including the PG itself, are added.
Click "Apply" — this will display all products associated with the PG and its members.
Select the relevant products as shown in step No. 5.
Finally, click "Add":

Now click "Save":

Note: The certification scope work order serves as the central repository for all information that will appear on the certificate. Therefore, it’s essential to ensure that the full certification scope is captured here—including all producer group members and their respective products as shown above.

With this, the system triggered the smart forms that have to be filled out for the certification scope work order. They can be seen under the respective tab:

From the Certification scope work order, you must create the QMS and member sample audits.
The QMS audit can be created following the steps below. Click on the clip icon -> Add link -> Add new item:

Under Link type select "Related" and under Item type select "Audits", name the QMS audit and press "Add link":

Click on continue:

Click on continue:

Under Reporting Option, select "Option 2 - Group Certification":

Under Audit type select one of the underlined options based on what is applicable in your case:

Select the applicable product category(ies):

Select the applicable audit address and submit:

With this, you have created the QMS work order:

Before you can start filling out the QMS WO smart forms, you have to add the PG's products to its scope by selecting the product tab and clicking on the "Add Product/Site/PHU" button:

Here again it is advised ot choose the "Advanced search" and follow the same steps as explained above. Important: Make sure you select under producer only the PG. With this, only the QMS-relevant products will be displayed. In this example, the PG and the PG's central PHU products appear:

After the above has been saved, the system triggers the necessary smart forms for the QMS audit, which can be seen under the respective tab:

When clicking on the clip icon in the right-hand side, you will see on the right-hand side the link to the initial certification scope work order:

To continue, you need to select the Certification scope work order to return to the starting point of this audit. From there, you can create the sample audits.

Press again "Add link" and "Add new item":

Select "Related" and "Audits" and name the sample audit:

Select "Option 2 - Member of Group Certification" and name the sample audit accordingly:

Click on continue:

Make sure you select the correct sampled producer group member and click continue:

Make sure you select the Reporting option: "Option 2 - Member of Group Certification", Audit type: "Audits for sites and members", and the applicable Audit Product Category(ies) applicable for each producer group member, and click on continue:

Click on Submit:

With this step, you’ve successfully created the sample work order for the producer member. Next, similar to the previous process, we need to include the producer products in the work order scope to ensure the system triggers the appropriate smart forms:

Please use the Advanced Search feature and follow the steps outlined below. At Step 3, ensure you select the producer who will be audited through this specific work order:

After the above is saved, the system will trigger the appropriate smart forms for this PG member work order, which can be seen under the respective tab:

Note: Producer group sample work orders need to be created for every sampled producer, always directly from the certification scope work order.

You're now set to begin the Option 2 audit. Please ensure that all smart forms are completed within each work order.

Below is a simplified diagram illustrating the Producer Group (PG) hierarchy. In this example, the PG manages its own production, operates a Central PHU, uses an External PHU, includes three PG members, and produces a total of three products.

Please note that in case the PG shall be audited/assessed against additional add-on Farm Assurance Products, they shall be connected to the IFA audit in the same way as above: Starting from the IFA Certification scope work order, you must create the Certification scope work order for e.g. GRASP. From this GRASP certification scope work order, you create the GRASP QMS and GRASP sample assessment work orders.

The same applies to any additional work order.

For additional information, find here the related recordings.

Audit Assignment Notifications on Mobile App

When an audit is assigned to the mobile app of an auditor, she/he will receive a push notification (pop-up message) if this feature is enabled on her/his device.

Please note that this feature has to be enabled on the device platform settings.

View all
How can we proceed if the same audits may be applicable to more than one scope?

Please note that one audit report (one work order) will contain the information for a single Farm Assurance Product. Therefore, only one audit type will apply per audit report.

Please note that multiple Audit Product Categories can be selected under the Plants scope. See below a random example:

If you create a Non-Conformance ticket, why does it not automatically add the level, i.e. Major, Minor, etc.? Does it give the due date for the NC to be closed?

It is a limitation of the system that you need to re-enter the level of the NC.

The due date has to be added manually to the smart form and NC ticket directly after raising the NC.

May two staff members contribute information regarding one Producer/audit?

Yes, more than one staff member can work on a work order. E.g., administrators can add general information, and the auditor will fill out the audit-related smart forms.

Through the mobile application, work orders can be split between auditors. In such cases, auditors must coordinate to prevent overlapping tasks.

View all
Certification cycle alignments in CertifierOS

This article applies to the following Farm Assurance Products whose valid-to dates need to be aligned with the main standard (IFA): GRASP,  FSMA, AH-DLL GROW and NURTURE.

It also applies to QS-GAP alignments with the QS Database and QS FIAS alignments with the main standard QS-GAP.

If you need to adjust the valid-to date, you have two options:

  1. Align it during the next audit or assessment, or
  2. Initiate a modification audit to update the valid-to date immediately following the launch of CertifierOS on 03/11/25.

To proceed with the modification audit, you must first create the producer’s site(s) and product(s).
If the alignment shall be done for a Producer Group (PG), this includes creating the sites and products for all PG members.

See here how to create a site.

See here how to create a product and add it to a site.

Note: Creating sites and their associated products is a one-time setup. This process does not need to be repeated for future audits or assessments.

To create the modification audit/assessment work order you need to select "+ Create" from the audit section in CertifierOS:

Select the applicable Farm Assurance Product and properly name the audit/assessment: and click continue:

In this random example we select a GRASP v2 assessment:

Select the producer and the contact person and click continue:

Now we need to select the

"Reporting option" (in this random example it is an option 1 single site)

The "Organization" (your CB)

Under "Audit type" we need to select "Modification audit"

Under "Audit Peoduct Category" we select the appropriate option. Note that only for GRASP "Non-applicable" is the correct option. For other FAPs, it can be F&V, F&O, AQ, etc.

Please also note that the "GRASP V2 - Checklist type" shall only be selected in case of a GRASP assessment. For all other FAPs this field shall remain empty:

We select the audit address and submit the work order:

With this we have created our modification scope work order. Now we have to select the "Products" tab:

And add the products to the certification/assessment scope

We click on "Advanced Search":

First click on the siphon icon, -> select "Product" -> Apply -> select the applicable product(s) -> click "Add":

Click Save:

With this, the system triggers the appropriate smartforms, which can be found under the checklist tab. The smart forms have to be filled out as explained in this recording. Please not you can also user the Attribute mass entry feature.

After the smart forms are filled out you need to close the smart form as closed compliant:

The next step is to issue the new version of the certificate/Letter of conformance via the certification section. Click on "+ New Certificate:

Under "Audit" select the audit/assessement you have just finalised, under "Status" depending on the FAP, either Certified or Assessed and under "Certificate Document Template" the applicable template. (Find here the instructions how to create your CB's certificate templates). You select the validity dates to align with the main certificate and click on "Generate"

How to create a GRASP assessement work order in CertifierOS

You can start preparing the GRASP work order either directly by clicking on "+ Create" or by linking it from an existing IFA work order.

To see how to create a GRASP work order from an existing IFA audit work order, please see this recording.

In this example, we will start the process by clicking on "+ Create".

In the pop-up window, select "GRASP V2" and assign an appropriate name to the assessment, following the example shown below:

As always, we select the producer and the contact person:

On the next pop-up window page, we will have to select:

The Reporting option, according to the situation. Here we selected an Option 1 - Single Site Certification

Our CB under "Organization"

The "Audit type", according to the applicable audit type. In this example, we selected "Initial certification audit"

The "Audit Product Category". In GRASP assessment work orders, we need to select "Non-applicable"

The "GRASP v2 - Checklist type" depending on the worker's situation on site. See the available options below. In this example, we selected "GRASP v2 - Hired/Subcontracted workers (Initial year)"

Please ensure that the field 'GRASP v2 - Checklist type' is used exclusively for GRASP work orders. If applied to other types of work orders, such as IFA, it will cause the system to trigger incorrect smart forms.

As always, we select the audit address and submit:

With this step, the GRASP assessment work order has been successfully created. The next action is to include the relevant product(s) within the assessment scope, as we do for any other Farm Assurance Product. We select the "Products" tab:

and click on "Add Product/Site/PHU"

In this example, the product is "Maria Carrot's (6291041011566) product carrot"

With this, the applicable smart forms for our assessment were triggered and can be seen in the relevant tab:

The remaining process is identical to any other Farm Assurance Product.

Issuing the GGFSA Add-on Letter of Conformance for Years 2 and 3

The process for the years two and three is based on the extension of the initial Letter of Conformance.
As in all cases, the initial Letter of Conformance needs to be created following the usual certification process in CertifierOS.


To proceed with the extension in year two, navigate to the certificate section in CertifierOS. Locate the original Letter of Conformance, click on the three-dot menu next to it, and select 'Edit' to begin the extension process:

Next, update the original validity end date by one year. To do this, click the calendar icon and choose the appropriate new date from the pop-up calendar. In this example, we change the date from 25/03/2026 to 25/03/2027.

Please note that the Letter of Conformance will be updated from version v1 to v1.1.


In the third year, the same procedure is followed. The new validity date will be set to 24/03/2027 in this example, and the certificate version will be updated to v1.2.

In the fourth year, a complete audit must be conducted and documented in CertifierOS, resulting in a new version of the Letter of Conformance—v2. For years five and six, the same extension process applies, leading to LoC versions v2.1 and v2.2, respectively, and continuing in the same pattern thereafter.

How to issue a certificate/Letter of conformance in CertifierOS?

After the audit/assessment is successfully finalised and the audit work order is closed as "Closed compliant",

we can issue the certificate/Letter of Compliance (LoC). To do so, we need to go to the certificate section and press on "+ New Certificate":

After clicking on the "Audit" field, in the pop-up window, we can select the applicable audit. Please note that here, all your CB's closed-compliant audits/assessments will be listed.

By clicking on the "Status" field, you can select the applicable status.

Please note that in case a certificate needs to be issued, the status "Certified" must be selected. In case a Letter of Conformance has to be issued, the status "Assessed" has to be selected.

The next step is to select the applicable certificate template by pressing into the relevant field:

In our example, we have selected "IFA v6 Plant - Option 1"

The next step is to select the validity dates and press "Generate"

How to audit Chain of Custody (CoC) in CertifierOS

To start a CoC audit, we need to create our certification scope. To do so, we first must create the producer’s product scope site. We start by selecting the Type “Sites/PHU”

Then we choose the category “CoC Scope Registration (Site)”:

Next step, as always, is to properly name the site. See here an example:

The next step is to select the producer:

Please note that the CoC Scope Registration (Site) does not require an address, as its purpose is solely to record the CoC certification scope.

After we finalise the site creation process, we proceed with adding the product(s).

We select under Type “Products”, we do not choose a Category and properly name the product. In this example, we will use “Plants”:

We select the producer:

The next step is to select the product.
Please note that the only products applicable for the Chain of Custody scope are:
Plants” (ID: 10940)

Aquaculture” (ID: 10941)

Compound Feed” (ID: 10942).

 In this example, we have selected plants:

As always, for a product, we need to select under "Parent" the respective site and CB:

In case this CoC producer is also handling Aquaculture and/or Compound feed, these products must be added to the “CoC Scope Registration (Site)” in the same way as seen above.

In case the CoC producer is operating a PHU or using an external PHU, we must create them accordingly by using the highlighted options below:

After the CoC PHU/External PHU is created, we proceed with adding the product.

For a PHU, we need to select the product “CoC PHU” (ID: 10943), and for an external PHU, we need to choose the product “CoC External PHU” (ID: 10944).

In this example, we select under Product “CoC PHU” and under "Parent" the respective PHU we just created:

To summarise, in our example, we have created,

  • a CoC scope site,
  • added product “plants” to the CoC scope site,
  • created a CoC PHU site,
  • added the product “CoC PHU” to the CoC PHU site:

Please note that the creation of the scope site and product scope needs to be done only for the first audit. For all future audits, the above process shall not be repeated, as the site and product can be reused.

After having finalised the creation of the scope and, if applicable, PHU/External PHUs and their respective product(s), we can start the audit in the same way as always by selecting the Farm Assurance Product (FAP).

For CoC audits, the following options are available:

Please note that for “GLOBALG.A.P. Chain of Custody (CoC) v6.1” the available scopes are "Plants", "Aquaculture" and "Compound Feed".

For “GLOBALG.A.P. Chain of Custody (CoC) v6.1 through BRCGS”, the available scope is "Plants".

 For “GLOBALG.A.P. Chain of Custody (CoC) v6.1 through IFS”, the available scopes are "Plants" and "Aquaculture", and

for “GLOBALG.A.P. Chain of Custody (CoC) v6.1 through QS”, the available scope is "Plants".

After selecting the FAP, the certification option, naming the audit and selecting the producer in the same way as in all other audits, we need to select the applicable Audit type, Audit Product Category and Checklist type.

Under Audit Product Category, we need to select “CoC scope” and under Checklist (CL) type, only in case of GLOBALG.A.P. Chain of Custody (CoC) v6.1, we have the following two options:
- CoC-SC Supply Chain v6.1

- CoC-RSRC Retail Stores and Restaurant Chains v6.1

Please note these two CL types only apply to GLOBALG.A.P. Chain of Custody (CoC) v6.1, so they shall not be used for the other CoC FAPs.

Note: For CoC via QS/IFS/BRCGS, the Checklist type shall not be selected.

In this example, we have randomly selected the CoC-RSRC Retail Stores and Restaurant Chains v6.1 CL type.

As always, we select the producer’s product scope:

Our example producer has two products, which we will select:

With this, the necessary smart forms were triggered, which must be filled out:

Please note that P&C smart forms are only available for CoC v6.1, CoC v6.1 through QS & CoC v6.1 through IFS.

A P&C smart form is not available for CoC v6.1 through BRCGS, as the necessary information in this case is documented via the BRCGS system.

Please note that in the Certificate Data smart form, the Species documentation is mandatory for Aquaculture. In the case of Plats or Compound feed, it is voluntary. In case you do not document a specific species, please mark it as “Non-applicable”:

After all the smart forms are filled out, and in case the audit was successful, the certificate can be issued in the same way as all the other FAPs. See this wiki for detailed instructions.

How to create certificate templates in CertifierOS

CBs must upload their own certificate templates to CertifierOS for every Farm Assurance Product (FAP) they certify. Each FAP and certification option requires only one template upload.

To do so, please follow the instructions below:

The CB has to download the relevant certificate template from this GLOBALG.A.P. SharePoint folder.

See here, for example, the certificate template options available for IFA v6 SMART Plants:

Via right-click on the three dots, select 'Download' to your PC. In this example, we have chosen the template for IFA v6 SMART Plants Option 2:

After opening the template, you will see that you can only amend the highlighted parts:

Please add under <CB Logo> your CB's logo and under "<accreditation mark> No. of certification body: ${Organization.OrganizationId}" your accreditation mark, including the accreditation number. The latter shall be added only for the applicable FAPs. In case you are not yet accredited for a certain FAP, please delete the relevant icon. (After the accreditation is achieved, you can amend your template by repeating this process.)

Note: You can find the correct document version by searching the related P&Cs in the document centre. In this example, this would be the related document:

Note: The document version is not mandatory for every FAP. If the template does not include a <document version> field, the document version shall not be entered.

The final template would look like this:

Please note that for several FAPs, the templates are prepopulated.

Before proceeding to the next step, please add the signature of the authorising person.

Note: For producers and PGs that do not operate a PHU, separate templates must be used. These templates can be found in designated subfolders for each FAP, as seen in the first screenshot above.

Note: In some cases, some parts of the templates will appear corrupted, similar to the below:

This is caused by a missing font on your PC. You can find the font in this folder. Please install it on your PC to fix this issue.

Please select in CertifierOS: the gear icon at the bottom left-hand side -> Global -> Document templates:

Now select "+ Upload Template":

Name your certificate template by filling in the "ID" and "Name" fields in the pop-up. Both fields can have the same value, as demonstrated below. Please note that clear template names will allow easy access during certificate issuance. The field "ID" can be used in accordance with the CB's own procedures.

Under "Usage Context", please select "Certificate".

Under "Orzanization" select your CB.

NOTE: DO NOT switch on the "Global Template" toggle

Click on the blue "upload" field or drag and drop the template from your PC, load the document and press "Upload":

You will see that the template you just created will appear at the end of your list:

By clicking on the three dots, you can download, delete or edit your template.

If you wish to edit, you can amend the "Name" and, by clicking on the "x", you will be able to upload a new template to replace the previous one.

Please note that any template change does not affect previously issued certificates.

To use the templates, please follow the known certification process:

Select the applicable "Audit", "Status" and "Certificate Document Template". In this example, "IFA v6 SMART Plants - Option 2"

Then press "Generate":

To view the generated certificate, navigate to the Certificate section. In the 'Certificate Template' column, you can identify which certificates are already linked to a template.

Select the certificate you want to view, then click the three dots on the right side and choose 'View' from the menu:

On the next page, click on "View PDF" to download the PDF certificate.

If the certificate template needs to be updated—for example, if an incorrect template was selected or the CB logo has changed—you can do so by selecting the relevant certificate, clicking the three dots, and choosing 'Edit':

A pop-up window will appear showing the template currently in use:

Clicking on the current template field will open a drop-down menu displaying all templates created by the CB. From there, select the appropriate template and click to apply it:

Click 'Save Changes' to generate the updated certificate. You can then download it following the steps described earlier.

This is the test certificate issued based on the above process:

Should the audit scope of an option 2 cover all Producer group members/products/PHUs or only sampled items?

Everything that needs to be listed on the certificate must be included in the Certification scope work order of the Option 2.

This includes all producer group members, PG's own fields (if applicable), all PHUs (central, external, and member), and all products.

CertifierOS Terminology

This wiki contains only the terms that have been newly introduced in the new GLOBALG.A.P. IT system platform.

  • External ID:

For the time being CertifierOS (CoS) is using the term "External ID" instead of the GGN or GLN. This will be amended in the future:

  • D-U-N-S Number

A "D-U-N-S Number" is an identification number similar to the GS1 system, and if available, it can be added to the producer's master data voluntarily.

The term "Organization" is used for "Certification body"

  • PG/multisite scope information (Site):

This is a "dummy" site/parent entity category that the system requires to introduce the PG's/Option 1 multisite with QMS scope into the certificate.

All the PG's/Option 1 multisite with QMS products need to be added to this "dummy" site.

  • Central PHU

"Central PHU" shall be used for the PHUs operating under the QMS of an Option 2.

  • Parent:

It is an item that has a hierarchy over another item.

E.g., a production site is a parent to a product that is produced on that side.

When creating a product, this is added to the "Parent". In this context, the "Parent" is the site where this product is produced.

A PG is a parent to a Producer Group Member.

When adding a producer group member to a PG, the PG is considered a "Parent" and the producer group member a "Child":

  • Sub Producer:

A Sub producer is a Producer Group Member

  • Work order:

A work order can be an audit report or the working file where the certification scope of a legal entity is managed. A work order contains one to several smart forms that define the contents and the purpose of the work order.

A work order is either a full or a part of an audit. Meaning it can be the complete audit for an option 1, or it can be, e.g., only the Certification Scope Management work order, or the QMS audit for a PG or a producer member audit/assessment.

  • Smart form:

Smart forms are checklists which contain either attribute questions or P&Cs.

  • Option 2 - Certification Scope Management work order:

For an option 2 certification, the system requires a central work order, which is called "Certification Scope Management" work order.

In this work order, the complete certification scope information for an Option 2 is collected and needs to include:

- PG’s certification scope

- Producer Group Members

- their product scope

- Producer group members' PHUs and their product scope (If applicable)

- PG’s Central PHU(s) and their product scope(s) (If applicable)

Please note that a certification can only be created from a single work order and not from a combination of several work orders. Therefore, the "Certification Scope Management" work order of an Option 2 will have to include all the information that is needed for the specific certificate.

The certification scope management work order is the basis of every PG audit, and it shall be the starting point for the creation of all work orders that are required to complete the audit:

- The QMS audit and

- the producer group member sample audits

  • Option 1 - Certification Scope Management multisite with QMS and Option 3 - Certification Scope Management multisite with QMS

In these work orders, the complete certification scope information for an option 2 multisite is collected and needs to include the information for the option 1, all its sites and PHU(s) (if applicable).

  • "Certification Scope Management" work order audit type:

This audit type is required for a) Option 2 - Certification Scope Management, b) Option 1 - Certification Scope Management multisite with QMS and c) Option 3 - Certification Scope Management multisite with QMS work orders. See example for a):

  • Scheduler:

The CoS functionality that allows the CB to assign audits/work orders to the mobile app of an auditor:

How can I suspend only one/some out many products in CertifierOS?

To suspend one or more products, they have to be removed from the certification scope via a modification audit.

After I amend a certificate on CertifierOS, I cannot see the "Date of Modification"

The "Date of Modification" will not be used in the new GLOBALG.A.P. IT Platform.

Instead, the combination of "Issue date" and Certificate Version will indicate the changes in the certification scope.

In CertifierOS, the initial certificate issued is assigned version number 1.
Each modification audit results in an incremental version, such as 1.1, 1.2, and so on.
When a recertification audit is conducted, the certificate version advances to 2.
Subsequent modification audits following the recertification will increment the version to 2.1, 2.2, etc.

Within the Database, the certificate expiry date is automatically generated by the system. Is it possible in the CertifierOS system to manually select or customize the certificate expiry date when making the certification decision?

Yes, this is possible.

How can I add a product to a PG member in CertifierOS during the certificate cycle when the certification has been made in the current GLOBALG.A.P. database? Would it be necessary to create sites/products for all the PG and all PG members?

A modification audit has to be created for the PG. The PG, all members, sites, PHU(s) and their product(s) need to be created and added to the certification scope work order. A work order for the affected producer group member has to be created and audited.

How do we handle cases, where the current certification cycle's "valid to" is before 03/11/2025, and a 4-month certification extension was requested by the client and the audit is planned after 03/11/2025?

In such cases, the Certification Body can enter the extension in the database before 31/10/25, while the audit should be prepared in the new IT platform. The certificate's "valid to" in the new system shall remain the same.

Will there be a PDF online certificate?

Yes, this feature is planned for a future update.

How can I add a new product to an existing certificate? Do I need to create a new work order and follow all the steps?

You will need to go to the existing certificate, press "Modify" which creates a new work order but with a copy of existing data, and then add the new product to the scope of the new work order.

Meaning in case of modification, it will be possible to create a new version of the audit with the same information that was filled in in the previous version. With this new version, a new scope can be assigned and a new version of a certificate can be created.

Please note that in case a certificate status was amended, e.g. suspended and reestablished, the modification audit functionality is not available. In this case, a new work order has to be created to include all information, including the new data. In case of Option 2, a new Certification Scope Work Order has to be created.

View all
A CB is the trustee of several GGNs in the database. Would this information be passed from the database to the new IT Platform automatically?

Yes, that is correct.

Will the PG/Producer with suspended products be transferred to the new IT platform?

Yes.

Will the previous activities in AOH be transferred to the new IT Platform?

No. Only the certificates and producer/PG master date will be migrated from the GLOBALG.A.P. database into the new IT Platform.

After the transfer to the new IT platform, do we have to create sites?

As the GLOBALG.A.P. database does not support site creation for the producers, the sites need to be created in the new IT System and be assigned to the producer.

Will all the attributes, sites, products, Geo-coordinates, etc. be transferred?

The legal entity master data will be transferred to the new system. Since there is no information in the GLOBALG.A.P. database about Sites, the complete data about SITES/PHU and PRODUCTS must be entered into the new system.
This can be done with the help of the bulk upload sheet or directly via the web user interface.

Note: The bulk upload sheet is shared in the CB-AT Portal.

Here is the direct link to the Bulk Upload Tool.

Will the previous Data from GLOBALG.A.P. Database be transferred to the new IT system?

The producer master data and certificates will be transferred.
Note: The products and their attributes will not be transferred.

View all
How to create a product and add it to a site/PHU in CertifierOS

Once you've created a site or PHU, as demonstrated in the link, proceed to the Products/Sites/PHU Browser section and click on '+Add Product/Site/PHU':

Under 'Type', we select 'Product' and properly name the asset and click on continue:

We select the producer and contact person to assign the product, and click on Continue:

We select the product under 'Product type'. You can find the product by typing into the search field, as seen below. Please make sure you start with a capital letter. In this example, we started typing 'Man..' to find the product 'Mandarin':

The next step is to select the applicable site under 'Parent'. When clicking into the search field, a drop-down with the sites of the particular producer will appear. By choosing the relevant site, we establish the connection between this product and that site:

We select our CB under 'Organization' and click on Submit:

With this, we have created the product and added it to its site. In this example, the product Mandarine that was assigned to the site 'Ben Johnson's site 1' that belongs to the producer 'Ben Johnson':

Note: via the hyperlinks you can directly reach the site and producer

How to create sites and PHUs in CertifierOS

Once you've created the producer or PG, as demonstrated in the respective links, proceed to the Products/Sites/PHU Browser section and click on '+Add Product/Site/PHU':

Select 'Site/PHU' at the 'Type' field:

Based on the scenario, choose one of the options under 'Category'. In this example, we select 'Site', properly name the site and click on Continue.

Note: The same steps apply to the other category options, as described in the following steps:

Note: Sites such as CoC, NON-GMO and SIZA sites are selected as described in the respective wiki articles.

We select the producer and the contact person to assign the site and click continue:

We select our CB under 'Orzanization' and click continue:

We either add the full address or the geo-coordinates of the site and click on 'Submit'.

Note: If the address is incomplete, the site will not appear on the certificate. When in doubt, it is recommended to use geo-coordinates.

For this example, we used random geo-coordinates and clicked on 'Submit':

With this, we have created the producer's site:

How to create a Compound Feed Manufacturing (CFM) v3.1 audit in CertifierOS

To start a GLOBALG.A.P. Compound Feed Manufacturing v3.1 audit, we need to create our certification scope. To do so, we first must create the producer’s product scope site. We start by selecting the Type “Sites/PHU” and afterwards one of the applicable "Sites/PHU and Category "GLOBALG.A.P. Compound Feed Manufacturing - Scope Registration (Site)":

As per standard practice, proper site naming is essential:

As always, we select the producer. In this example, it is the producer “CFM Test Producer”:

Please note that adding a contact person is not required.

We do not add a Parent; we select our CB under organization and submit. As always, you can add tags or a description to the respective fields. Please note that for the scope site, an address is not required:

The next step is to add the certification scope (product) to the site above.

The available products for this FAP are:

“Compound Feed for Aquaculture” (ID: 10949) &

“Compound Feed for Livestock” (ID: 10950)

As always, we select Type “Product” and properly name it. In our example, the certification scope is “Compound Feed for Aquaculture”:

We select the producer:

In our example, we will select the product “Compound Feed for Aquaculture” (ID: 10960), select under Parent the site we have created before, add our CB under Organization and press on submit:

We select the parent and submit:

Note: This standard does not require a PHU.

To summarise, in our example, we have created,

  • A CFM scope site,
  • Added product “Compound Feed for Aquaculture” to the scope site.

Please note that the creation of the scope site and product scope needs to be done only for the first audit and can be used for all future audits.

After having finalised the creation of the scope, we can start the audit in the same way as always by selecting the Farm Assurance Product (FAP). First, we select the relevant FAP and the applicable reporting option:

 In our scenario, we select Option 1 - Single Site Certification. Proper audit naming is essential:

We select the producer and contact person:

We select our CB, and under Audit type, we select the applicable option. In our example, we selected “Initial certification audit”.

Note: for all GLOBALG.A.P. Compound Feed Manufacturing v3.1 audits, under Audit Product Category, we shall select “GLOBALG.A.P. Compound Feed Manufacturing scope”:

We click through the pop-up window by clicking “Continue” and “Submit” the audit.

The next step is to add the Scope information to our audit:

&

With this, the proper smart forms will be triggered:

Please note that during the creation of this wiki, the P&C smart form was not available. This is the reason it is not displayed in the above screenshot.

After filling out the smart forms and finalizing the audit, the certificate can be issued as explained in this wiki.

If an option 1 producer has e.g., IFA, GRASP and SPRING  - do we have to create 3 work orders? And do we have to create the sites and their products for each standard separately?

In this case, three distinct work orders must be created-one each for IFA, GRASP and SPRING. The process begins with the creation of the IFA work order, from which the GRASP and SPRING add-on work orders will be subsequently generated and linked.

Please note that the sites and their products must be created only once for the producer and can be used for all applicable Farm Assurance Products, and also for all future audits/assessments.

Is the creation of a site (and PHU in case of product handling) obligatory for every producer also for benchmarked schemes?

Yes, all sites and PHUs (if applicable) and their respective products need to be created.

How to create an option 2 audit in CertifierOS

For a new Option 2, you need to create a parent site "PG/Multisite scope information (Site)" and assign all products of this PG to this parent site:

Note: The process for adding the product(s) to the "PG/Multisite scope information (Site)" is identical to the process for creating any other product.

In case the PG operates a PHU under its QMS, you need to create a "Central PHU" and add to it any applicable product(s):

If the PG is using an external PHU, this site must also be created. The Site Category in this scenario is "External PHU".

Note: The above assets have to be created only once and can be used for all future audits.

Before you can add members to the producer group (PG), you must first create the members themselves, set up their respective sites, and create and assign their products to those sites. The producer creation is shown in this recording, and the site and product creation can be seen here and here, respectively.

After our members are created, we can add them to the PG. We go to our PG and click on "+ Add entry:

You can search for the producer group members by GGN or name. You select via the tick boxes and press "Add":

In this example, we selected two producer group members:

If the PG has its own production, she must also be added as a member, following the same procedure described above.

Once the above steps are completed, the members will appear under the PG's producer hierarchy:

Now we can start preparing the required work orders. The first work order (WO) that needs to be created is the "Option 2 - Certification scope Management" WO, as seen below. We first select the applicable FAP and properly name the audit:

We select the PG and the contact person:

As this is the Certification Scope WO, under "Reporting Option", we must select "Option 2 – Certification Scope Management". Then, under "Organization", choose your CB. For "Audit Type", select "Certification Scope Management", and under "Audit Product Category", choose the applicable option(s) and click on Continue. In this example, we’ve selected Fruit & Vegetable, as shown below:

We select the audit address and click on Submit:

With this, we have created our certification scope work order. Now we have to add our producer group members and products by clicking on the respective tabs:

To add the members, we click on "Add New":

Select the producer by searching using their name, GGN, or the Advanced Search. Once all members have been selected, click "Save". Please also ensure that the PG is added as a member if it has its own production:

In the next step, we need to add the product by selecting the respective tab and clicking on "Add Products/Site/PHU:

It is advised to select the "Advanced search":

To include products in the scope, follow these steps:

Click the siphon icon.
Select the Type as "Product".
Ensure that all PG members, including the PG itself, are added.
Click "Apply" — this will display all products associated with the PG and its members.
Select the relevant products as shown in step No. 5.
Finally, click "Add":

Now click "Save":

Note: The certification scope work order serves as the central repository for all information that will appear on the certificate. Therefore, it’s essential to ensure that the full certification scope is captured here—including all producer group members and their respective products as shown above.

With this, the system triggered the smart forms that have to be filled out for the certification scope work order. They can be seen under the respective tab:

From the Certification scope work order, you must create the QMS and member sample audits.
The QMS audit can be created following the steps below. Click on the clip icon -> Add link -> Add new item:

Under Link type select "Related" and under Item type select "Audits", name the QMS audit and press "Add link":

Click on continue:

Click on continue:

Under Reporting Option, select "Option 2 - Group Certification":

Under Audit type select one of the underlined options based on what is applicable in your case:

Select the applicable product category(ies):

Select the applicable audit address and submit:

With this, you have created the QMS work order:

Before you can start filling out the QMS WO smart forms, you have to add the PG's products to its scope by selecting the product tab and clicking on the "Add Product/Site/PHU" button:

Here again it is advised ot choose the "Advanced search" and follow the same steps as explained above. Important: Make sure you select under producer only the PG. With this, only the QMS-relevant products will be displayed. In this example, the PG and the PG's central PHU products appear:

After the above has been saved, the system triggers the necessary smart forms for the QMS audit, which can be seen under the respective tab:

When clicking on the clip icon in the right-hand side, you will see on the right-hand side the link to the initial certification scope work order:

To continue, you need to select the Certification scope work order to return to the starting point of this audit. From there, you can create the sample audits.

Press again "Add link" and "Add new item":

Select "Related" and "Audits" and name the sample audit:

Select "Option 2 - Member of Group Certification" and name the sample audit accordingly:

Click on continue:

Make sure you select the correct sampled producer group member and click continue:

Make sure you select the Reporting option: "Option 2 - Member of Group Certification", Audit type: "Audits for sites and members", and the applicable Audit Product Category(ies) applicable for each producer group member, and click on continue:

Click on Submit:

With this step, you’ve successfully created the sample work order for the producer member. Next, similar to the previous process, we need to include the producer products in the work order scope to ensure the system triggers the appropriate smart forms:

Please use the Advanced Search feature and follow the steps outlined below. At Step 3, ensure you select the producer who will be audited through this specific work order:

After the above is saved, the system will trigger the appropriate smart forms for this PG member work order, which can be seen under the respective tab:

Note: Producer group sample work orders need to be created for every sampled producer, always directly from the certification scope work order.

You're now set to begin the Option 2 audit. Please ensure that all smart forms are completed within each work order.

Below is a simplified diagram illustrating the Producer Group (PG) hierarchy. In this example, the PG manages its own production, operates a Central PHU, uses an External PHU, includes three PG members, and produces a total of three products.

Please note that in case the PG shall be audited/assessed against additional add-on Farm Assurance Products, they shall be connected to the IFA audit in the same way as above: Starting from the IFA Certification scope work order, you must create the Certification scope work order for e.g. GRASP. From this GRASP certification scope work order, you create the GRASP QMS and GRASP sample assessment work orders.

The same applies to any additional work order.

For additional information, find here the related recordings.

How to Amend Work Orders When Audit Findings Require Changes


If an auditor discovers missing information during an audit (like an undeclared PHU or crop that wasn't mentioned in the initial application), the work order must be replaced.

To make these changes, you'll need an internet connection. Add all information, including the new information, e.g. in this scenario, create the PHU entries and their products. Once everything is updated, start a new audit using the corrected information.

The same applies also in the case of a GRASP assessment other conditions apply compared to the application (e.g. a family farm was expected, but hired workers are present at the farm)

Please note that the aforementioned actions cannot be performed via the mobile app.

CertifierOS Terminology

This wiki contains only the terms that have been newly introduced in the new GLOBALG.A.P. IT system platform.

  • External ID:

For the time being CertifierOS (CoS) is using the term "External ID" instead of the GGN or GLN. This will be amended in the future:

  • D-U-N-S Number

A "D-U-N-S Number" is an identification number similar to the GS1 system, and if available, it can be added to the producer's master data voluntarily.

The term "Organization" is used for "Certification body"

  • PG/multisite scope information (Site):

This is a "dummy" site/parent entity category that the system requires to introduce the PG's/Option 1 multisite with QMS scope into the certificate.

All the PG's/Option 1 multisite with QMS products need to be added to this "dummy" site.

  • Central PHU

"Central PHU" shall be used for the PHUs operating under the QMS of an Option 2.

  • Parent:

It is an item that has a hierarchy over another item.

E.g., a production site is a parent to a product that is produced on that side.

When creating a product, this is added to the "Parent". In this context, the "Parent" is the site where this product is produced.

A PG is a parent to a Producer Group Member.

When adding a producer group member to a PG, the PG is considered a "Parent" and the producer group member a "Child":

  • Sub Producer:

A Sub producer is a Producer Group Member

  • Work order:

A work order can be an audit report or the working file where the certification scope of a legal entity is managed. A work order contains one to several smart forms that define the contents and the purpose of the work order.

A work order is either a full or a part of an audit. Meaning it can be the complete audit for an option 1, or it can be, e.g., only the Certification Scope Management work order, or the QMS audit for a PG or a producer member audit/assessment.

  • Smart form:

Smart forms are checklists which contain either attribute questions or P&Cs.

  • Option 2 - Certification Scope Management work order:

For an option 2 certification, the system requires a central work order, which is called "Certification Scope Management" work order.

In this work order, the complete certification scope information for an Option 2 is collected and needs to include:

- PG’s certification scope

- Producer Group Members

- their product scope

- Producer group members' PHUs and their product scope (If applicable)

- PG’s Central PHU(s) and their product scope(s) (If applicable)

Please note that a certification can only be created from a single work order and not from a combination of several work orders. Therefore, the "Certification Scope Management" work order of an Option 2 will have to include all the information that is needed for the specific certificate.

The certification scope management work order is the basis of every PG audit, and it shall be the starting point for the creation of all work orders that are required to complete the audit:

- The QMS audit and

- the producer group member sample audits

  • Option 1 - Certification Scope Management multisite with QMS and Option 3 - Certification Scope Management multisite with QMS

In these work orders, the complete certification scope information for an option 2 multisite is collected and needs to include the information for the option 1, all its sites and PHU(s) (if applicable).

  • "Certification Scope Management" work order audit type:

This audit type is required for a) Option 2 - Certification Scope Management, b) Option 1 - Certification Scope Management multisite with QMS and c) Option 3 - Certification Scope Management multisite with QMS work orders. See example for a):

  • Scheduler:

The CoS functionality that allows the CB to assign audits/work orders to the mobile app of an auditor:

How to fix a site creation error

If an incorrect "Type" or "Category" is selected during site creation, these fields cannot be modified.

Non-editable information is displayed in grey:

In case the information you need to correct is greyed out you will need to rename this asset and clearly mark it as invalid. In this example, it would be renamed into: "Melon producer 2 (6291041011436) site - INVALID due to mistake"

I cannot see the contact person

In case you are trying to create a site/PHU/product and the producer's contact person does not appear, please select the producer via the "Advanced search" as seen below:

In case of an option 1 multisite, do I need to create e.g. all 3 sites? Then I would need to create and add a product for each site, right? And finally I add all to the Scope information?

Yes, that is correct. In this instance, all three sites must be created, and the corresponding product(s) for each site must be created and appropriately assigned to their respective locations.

During the preparation of the Certification Scope work order, all products have to be added to the certification scope.

Please note that, depending on whether the Option 1 multisite producer is operating a QMS or not, the applicable certification option shall be selected (Option 1 multisite with or without QMS).

If a producer for example has IFA/GRASP and CoC  - do we have to create 3 workorders? Do we also have to create the products for each standard separately?

One work order per Farm Assurance Product (standard/add-on) shall be created.

The sites and products do not have to be created per work order. They need to be created for the particular producer once and can be used indefinitely for all applicable audits/assessments.

Examples:

OPTION 1

In case an option 1 is going to be audited/assessed against IFA & GRASP & SPRING, three work orders have to be created:
One for IFA

One for GRASP and

One for SPRING

OPTION 2:

In case a PG is going to be audited/assessed against IFA & GRASP & SPRING, the following work orders have to be created:

IFA: 1) One Certification Scope work order, 2) one IFA QMS work order and 3) the required number of sample PGM audit IFA work orders (as many as the sampling of the PG dictates)

GRASP: 1) One Certification Scope work order, 2) one GRASP QMS work order and 3) the required number of sample PGM GRASP audit work orders (as many as the sampling of the PG dictates)

SPRING: 1) One Certification Scope work order, 2) one SPRING QMS work order and 3) the required number of sample PGM SPRING audit work orders (as many as the sampling of the PG dictates)

How to name sites, PHUs, products and audits

Under "Name", you can name the sites, products, PHUs or audits according to your needs. Using clear and consistent naming will make it easier to identify these assets when creating work orders.

In practice, we suggest naming in a way like this:

- Sites: "Producer name & GGN & Site XYZ". E.g.: "Max Mustermann, 4041234566789, Cherry River Site"

- PHUs: "Producer name & GGN & PHU XYZ". E.g.: "Max Mustermann, 4041234566789, PHU one"

- Products: "Producer name & GGN & example product name for Site XYZ". E.g. "Max Mustermann, 4041234566789, Cherry product for Cherry River site"

- Audits: "Producer name & GGN & audit type & date". E.g.: "Max Mustermann, 4041234566789 IFA F&V Cherry Smart recertification audit, 19/10/25" or another example: "Max Mustermann, 4041234566789 IFA F&V Smart extension to Fig audit, 16/08/26"

Does the registration process for sites/PHUs/products need to be completed every year?

No. Sites/products/(central)PHU(s) can be used indefinitely as long as they do not change.

For example, only if a new product is to be added to the certification scope, it has to be created and added to its respective site. The same applies for new site(s) and PHU(s)

How are PGs with own production handled?

In case the producer group has production of its own, the PG will be treated like a member. Meaning that it will be assigned as a member of its own producer group and products produced by the PG will be entered in the system the same way that it is done for the members of the PG.

View all
How to add Farm Assurance Products to an auditor user (FAP approvals) in CertifierOS

To add the FAP an auditor is assigned to, the Scheme Manager has to select the auditor and press "Edit":

Scroll down to "Audit Specific Details" and press "+Add":

Either scroll through the Farm Assurance Products to select the applicable:

Or type in the one you are looking for and click on it:

Then click on the Reporting Option field and select the applicable options (multiple selection is possible):

Make sure you have selected the applicable FAP and options before you press "Save"

Repeat the process to add the FAPs the auditor has approval for.

Please note, to remove a FAP from an auditor user profile please click on the "x" on the right hand of the respective FAP:

Can the scheme manager assign access credentials?

Yes. See here the relevant instructions.

Can the producer information or a CL for the auditor be prepared by a back-office worker/assistant?

Yes, these actions can be performed by the back office. Users will need to have the role "CB Assist / Audit Scheduler"

Are there any restrictions to view external audits by other auditors, etc.?

Users assigned the "Auditor" role in CertifierOS will have visibility into all audits within their respective CB.
This functionality is expected to be further enhanced in future updates.

Is it possible for another auditor to follow up corrective actions on the platform?

Yes, it is possible.

Will we continue to create the auditors in CB-AT? And will they appear in the CertifierOS after being approved?

CB-AT will remain operational to support auditor approvals.

Initially, CB-AT will not be connected to the new IT platform. All users of the new platform must be created directly in CertifierOS. Each CB's Scheme Manager (SM) will have the necessary permissions to create new users, following the instructions provided here.

Integration between CB-AT and the new IT platform is planned for a future development phase.

Can the reviewer and the certifier be the same person?

Yes, this has previously been permitted in the Audit Online Hub as well.

Is the GAIN-number automatically assigned to a certifier?

No, due to a limitation of the system. When the connection to CB-AT is established, GAINs will be assigned automatically.

Can the auditor create own audits, or do they need to be assigned?

Both alternatives are possible.

Will each role provide access for a different activity done in the CertifierOS?

There will be different levels of access to the system per role (e.g. Auditor or Scheme Manager) and each role will have the ability to view/edit information on the platform (or not see certain information at all).

Roles and Rights:

Scheme Manager, CB Assist / Audit Scheduler, Auditor (Farm or QMS), Reviewer / CB Committee, Signatory and Onsite Auditor (mobile role).

CoC and CFM auditors are not registered in CB-AT. How does this apply to this tool?

CoC and CFM audits will still be possible in CertifierOS, despite this limitation in CB-AT.

Find the Chain of Custody (CoC) wiki here.

Find the Compound Feed Manufacturing (CFM) wiki here.

View all
When using the upload sheet, can we register a producer with only the coordinates, or is it necessary to include the address as well?

Initially, the upload sheet will be used only for creating and modifying sites/products/PHUs. For sites & PHUs, Geo-coordinates are requested by the standard.

Producers have to be created via the webform or an API and require an address.

Would it be possible to have an Excel file to perform the audit in order to upload it to the CertifierOS?

Currently, the bulk upload sheet will only allow for the creation & modification of sites & products.

The audit process in CertifierOS does not support Excel file uploads.

Is it possible to see the process of the upload of the upload sheet?

Related recording shall be shared soon.

After uploading the Excel upload sheet, will we receive a confirmation message if everything is correct, or an error message in case of an incident?

The program will first validate that all information is in the correct format. In case there are any errors in the format, the exact cell in the worksheet will be marked along with a note explaining what is wrong. After uploading the sheet, any GGNs which could not have their data uploaded will be marked, along with the error message.

Are there any limitations on the size of the upload sheet?

No, the upload sheet size is not limited.

Do we need to add separate lines to the upload sheet for each product of the producer?

Correct, each line must be a different product, regardless of the option of the producer. The only case where this is not true is when the producer is auditing the products for a standard and one or more addons. In this case, the products must be repeated, along with a separate scheme ID.

Where do I document the countries of destination?

The countries of destination will need to be filled out in the site attribute smart forms. See here a random example:

How to upload the upload sheet? How do I get access to the upload tool?

A dedicated software will be provided by the Secretariat. It shall be installed on your computer. The upload sheets will be uploaded to the system via this software.

Note: The bulk upload sheet is shared in the CB-AT Portal.

Here is the direct link to the Bulk Upload Tool.

Will the bulk upload sheet be available to test in PREPROD?

Yes, it will be available to test in PREPROD.

Will the O-keys of the CBs and PGs still be used in CertifierOS or in the new mass upload sheet?

Only the Organisation ID (previously the o-key) of the CB is necessary for the upload sheet.

Is the CB ID, that is needed in the upload sheet, the current O-key from the Database?

Yes, that is correct. This ID is the Organisation ID, which can be found in the web interface.

What can I do with the upload sheet?

For the time being, the upload sheet can be used to create new/amend sites/PHUs, Products, and link the products to their respective sites/PHUs.

In the future, the upload sheet will be used in addition to the above to create new producers/PGs, link the PG members to the PG, create audits and issue certificates.

Where can I find the upload sheet?

The upload sheet is stored in CB-AT Portal.

Here is the direct link to the Bulk Upload Tool.

View all
In case we use an API, can we register Producers, sites/PHUs/products, then create the work order and make the connections and finally complete on our local platform the smart forms required for the work order after the audit date and submit everything to OSAPIENS at the time of certification?

Yes, this is possible.

Will we be able to upload also the audit reports through a template?

Yes, this can be done via the API.

Auditors will be able to complete P&Cs offline on the mobile app. Will they be able to use an Excel template created by the CB in their native language, given that the system is only in English?

Yes, this can be done via the API.

To create a new audit via the API interface (based on this), information such as ‘country’, ‘city’, ‘postalCode’ and ‘houseNumber’ must be sent (Mandatory=yes). Why is it not sufficient to send just the LocationID of the Audit site?

This is a limitation of the system. If you only send the locationID, the address and other details deemed mandatory will not be registered in the report.

Is the API environment at https://preprod.osapiens.cloud/data/integration/ still connected to the portal at https://preprod.osapiens.cloud/portal/portal.html?

Yes, it is.

Using our own platform and your API, can we import a whole workflow on the complete status, or do we have to log all the steps of the audit in different time periods?

You can import the whole process at once. Notice, however, that the answers to the smart forms need to be submitted via separate API calls, non-conformance tickets need to be created and assigned separately, and there is a specific call for the work order status change.

When will the final version of API documentation be issued, so that the IT developers can proceed?

IT developers can proceed with implementation immediately. The API documentation is continuously updated (similar to how the AOH API documentation was regularly refined). Substantial documentation is already available, and no significant changes to the core documentation are anticipated.

When using API, at which time point will the audit be communicated to the online platform?

From an API perspective, at any point in time you can send the data via the API.

Will it be possible to retrieve our CB data uploaded/updated via API (e.g., to check fee calculation and data for certificate issuance/validity)?

Certificate data can be retrieved through the API.

For certification bodies which use a third party software, will the API continue to work with CertifierOS?

Yes, API support will be provided, and the documentation can be found here.

View all
Is there a procedure for the non-conforming GRASP P&Cs that also affect particular IFA minor must P&Cs and elevate them to major musts?

There is no technical integration between IFA and GRASP, nor between any work orders that would enable such cross-verification. The GRASP checklist will ask if the particular IFA worker welfare P&Cs have been complied with.

How can we link the Add-ons to IFA audit?

See here the option 1 and option 2 recordings on how to link a GRASP v2 add-on to the main IFA audit.

Please note that linking all add-ons (not only GRASP) to the main audit is handled in the same way.

The linking process always starts from the main audit work order (In case of an option 2 audit, linking an add-on work order must be done from the IFA Certification Scope Work Order).

We start by pressing the Clip icon on the right-hand side to expand the banner, then pressing "Add link" and then "Add new item":

At the pop-up window, select under Link type, "Related", under Item type "Audits" and name the audit according to the selected FAP and producer, and press "Add link". See below a GRASP example:

The next screen will display under the Farm Assurance Product field the FAP from the work order that the process started. In this example, it was an "344002 - GLOBALG.A.P. IFA version 6 SMART - Plants" work order:

We need to delete this FAP and select the applicable one. In this random example, we select a GRASP v2 assessment. We also need to select the applicable Reporting option and press "Continue":

In the next screen, we select the producer and contact person and press "Continue":

In the next screen, we select the highlighted fields below according to the FAP work order we want to create. See the wiki links at the end of this article, which explain the differences per FAP:

In this random GRASP v2 work order example, we selected the following options:

The next screen requires adding the audit address:

In the next screen, clicking Submit creates the linked work order, which can then be audited like any other work order:

Please note that only for the GRASP add-on, the "Audit product category" "Not applicable" must be selected.

For GLOBALG.A.P. Compound Feed Manufacturing v3.1, the "Audit product category" "GLOBALG.A.P. Compound Feed Manufacturing Scope" must be selected. See here a detailed description of how to set up a Non-GM audit.

For GLOBALG.A.P. NON-GM/Ohne Gentechnik, the "Audit product category" "GLOBALG.A.P. NON-GM/Ohne Gentechnik Scope" must be selected. See here a detailed description of how to set up a Non-GM audit.

Find here instructions on how the GLOBALG.A.P. Chain of Custody work order shall be created.

For all other add-ons, the applicable "Audit product category", e.g. "Fruit & vegetables", shall be selected.

In case of GRASP, where do we upload the LoC?

The LoC will be generated automatically by the IT platform after the assessment is finalised.

How does the IFA+GRASP (or any add-on) look like: separate checklists or one by one?

Each Farm Assurance Product (FAP) requires separate work orders, which contain the applicable smart forms (P&C CL & attribute documentation) per FAP and need to be filled out separately.

Combined audits shall be linked. Find here the relevant recordings for Option 1 and Option 2 GRASP v2.

Please note that all add-ons shall be linked to the main IFA audit in the same way.

How is an Add-on Audit/Assesment created?

Find here the recordings for GRASP v2 option 1 and option 2.
All add-ons can be linked to the IFA audit in the same way.

View all
What is the procedure for the benchmarked schemes?

The process will be very similar to the process presented for IFA. In case of benchmarked standards, there will be less information to be completed before issuing a certificate (The P&C checklist of the benchmarked schemes shall not be filled out in the new GLOBALG.A.P. IT platform).

How should CBs that operate a Benchmarked Scheme, issue Option 3 certificates CertifierOS, and utilize their own Benchmarked Scheme Certification Application and Portal?

CBs must use CertifierOS as they do for options 1 and 2; however, they will select reporting options 3 or 4 instead. This will automatically trigger the relevant smart forms that need to be completed. Please note that benchmarked P&C checklists will not be triggered.

How does the CertifierOS it work for option 3?

Similar to option 1, you'll implement the same approach but will select reporting options that begin with "Option 3."

Please note that benchmarked schemes in this scenario won't include any P&C checklists that need completion.

See here a random benchmarked scheme example:

View all
Will there be specific training videos available for Chain of Custody?

The related recording shall be shared soon.

As an alternative, find her the related Wiki.

Can we create demo audits to test?

Yes. Please use the preprod-external/ test environment for testing purposes. In case you are experiencing any issues logging in, please contact the Stakeholder Helpdesk.

If we want to practice, can we create producers and PGs and delete them afterwards?

Feel free to test only in the Test (Preprod) environment.

Producers and PGs can be deleted. The ability to delete sites and products will be introduced in a future update.

Can you summarize the certification process in the new IT System Platform?
  • The producer had to be created/updated.
  • All his/her site(s) & PHU(s) and products have to be created.
  • The product(s) have to be linked to the respective site(s) and PHU(s).
  • The audit has to be created, which will trigger the relevant P&C and attribute checklists (smart forms) according to the FAP, certification scope and reporting option.
  • The audit needs to be assigned to the auditor(s). 
  • The auditor(s) need to complete all checklists (smart forms) and close the NCs if applicable.
  • The CB has to review the audit and take the certification decision by filling out the relevant smart forms. 
  • The CB issues the certificate.
How do I obtain credentials to access the test (pre-production) environment?

Please contact customer_support@agraya.com.

Your request shall include the new users':

  • Surname(s),
  • name(s),
  • e-mail address(es),
  • GAIN(s),
  • Farm Assurance Products they are assigned for (E.g. IFA F&V, GRASP, SPRING, etc.),
  • The certification option the auditors are approved for (Option 1/2).

If you are requesting credentials for multiple users, please provide the required information in an Excel file.

What is the URL of the test environment where the entire process can be viewed and tested?

Find here the preprod (test) environment: https://preprod.osapiens.cloud/portal/portal.html

How to proceed if I face any challenges in the system, e.g. in creating a checklist and audit?

You can find the training videos here.

If you still face any challenges, please share the details with our Stakeholder Helpdesk Team. Please make sure to share the producer/PG name, GGN, audit ID, CertifierOS environment (Live or preprod) and related screenshots.

View all
Mobile App Onboarding Instructions for iOS Devices (iPhones & iPads. Mac books are not supported)

Prerequisite: The user has a license key available and a user in the CertifierOS portal
Note: Depending on the device and software version, the user experience may differ
from the one described below

PREPROD Environment

  1. Install the mobile application for testing in PREPROD environment. The
    application is available in the App Store: osapiens HUB for Service PP in
    App Store

    a. Note that the application needs to be installed directly on the device
    where the application is intended to be used
  2. Once the application has been installed, open the application
  3. Enter the license key and select “Activate Device”
  4. In the next screen, select “Synchronize” so that organizational settings of your
    CB are imported
  5. Enter the username and password of the user who will use the mobile
    application. The username and password are the same that are used to log in to
    the online portal for Certifier OS
  6. The user should now see the audit overview screen and the different audits that
    have been assigned to the user

LIVE Environment

  1. Install the mobile application for use in the LIVE environment. The application is
    available in the App Store: osapiens HUB for Service in App Store
    a. Note that the application needs to be installed directly on the device
    where the application is intended to be used
  2. Once the application has been installed, open the application
  3. Enter the license key and select “Activate Device”
  4. In the next screen, select “Synchronize” so that organizational settings of your
    CB are imported
  5. Enter the username and password of the user who will use the mobile
    application. The username and password are the same that are used to log in to
    the online portal for Certifier OS
  6. The user should now see the audit overview screen and the different audits that
    have been assigned to the user
Audit Assignment Notifications on Mobile App

When an audit is assigned to the mobile app of an auditor, she/he will receive a push notification (pop-up message) if this feature is enabled on her/his device.

Please note that this feature has to be enabled on the device platform settings.

How to assign an audit to an auditor

In case the audit is programmed to be audited via the mobile app, you can drag and drop the audit work order(s) to the selected auditor via the Scheduler section in the web portal.

Via "Search by name" and "Search for Audit ID or Title, you can easily filter out the auditor and work orders.

Please note that you can drag and drop by clicking on the 6 dots right next to the audit ID. Once an audit work order is assigned, the six dots are no longer visible.

Once the audit work order is assigned to the auditor, click on it to activate it. Then, select "Release Selected" to send the audit to the auditor's mobile app. You’ll notice the audit work order changes to a darker colour, indicating it has been successfully released.

If needed, you can withdraw the audit work order from the auditor by right-clicking and selecting "Delete".


For assigning work orders to the mobile app, find additional information here.

To assign the audit work order via the portal, press the two people icon on your right-hand side:

Press on "Add member"

Select the applicable role by pressing on the first field of the pop-up window:

Select the applicable person from the second field:

You can filter out the applicable person by typing her/his name.

Auditors who are working for more than one CB do not appear in the CertifierOS Scheduler

Auditors working with multiple CBs will only appear in the Scheduler of their designated 'Main Organisation' (CB).

The 'Main Organization' can be amended by the CB's Scheme manager in case the auditor does not appear in the Scheduler.

To do so, please go to the users section and select the applicable auditor by clicking on the three dots at the right-hand side:

Scroll down to the 'Main Organization' and, in case this field is empty, select your CB as seen below:

This action is required each time an auditor needs to audit for a different CB via the mobile app.

The web interface remains unaffected by this limitation.

Will the new IT platform also apply to non SMART audit types (e.g., IFA v6 GFS)?

All Farm Assurance Products, including the GFS versions, all add-ons and Benchmarked schemes shall be audited via the new GLOBALG.A.P. IT platform.

How does the mobile app work?

If there is no internet connection available, auditing should be conducted offline using the mobile application.
Find here the related instructions on how to install the application, and a recording on how to use the application.

After an audit is assigned via the portal, as explained here, the mobile app has to be synchronized while being online. The position of the grey synchronisation button on the top right-hand might differ depending on the platform. During the synchronization, a green moving circle will be visible as seen here in the top center:

The audits (work orders) assigned for the particular auditor will be visible on the left-hand side of the app after synchronizing. All new ones have the status "open":

By tapping the syphon icon at the top center, the auditor can access various filter options—shown here—for quick and easy navigation of work orders.

Once the desired work order is activated, the left-hand border will turn green to visually confirm the activation.
By clicking on the three dots, the auditor has the option to reject or assign the audit to another auditor:

To proceed, the auditor shall press on "Start Work" and "In Progress":

The refreshed interface displays the number of smart forms included in the work order, along with dedicated sections for comments, images, and documents. In this test case, the work order contains 7 smart forms.

When a Smart Form is activated by clicking on it, it will appear on the right-hand side of the screen. All forms are currently in the 'open' status.

When a Smart Form is activated by clicking on it, the overview shifts to the left-hand side, while the corresponding attributes or P&Cs—depending on the selected form—are displayed on the right-hand side.

Clicking on 'Show more' reveals the compliance criteria and an explanation of the audit method. To hide this information, simply click 'Close'.

Once all P&Cs in a section have been completed, the yellow 'In Progress' label will change to a green 'Done' status. Comments must be provided in accordance with the GRs. To proceed to the next section, click 'Next →' located at the bottom right corner.

If an NC is raised, an additional field will appear below the comment section, prompting the user to enter a due date. To generate the NC ticket, click the yellow 'Create' button.

Enter the relevant information. Please note that fields such as 'Corrective Actions' and 'Closed By' should only be completed after the corrective actions have been received, in line with accreditation requirements.

If you're using a device with a camera, you can capture images by clicking on 'Images'. These photos will be automatically attached to the NC ticket, serving as evidence of the non-conformity.

After pressing the green "+", you will be able to take new pictures or select from your device's gallery:

To store the NC ticket, press "Save". To return to the P&C CL, press the green arrow:

You will see that the NC ticket changed colour and now appears in light blue.

After synchronizing, the NC ticket will be available in your browser view in the right-hand banner of the respective work order under the connector icon. In case you are using the mobile app with an internet connection, the NC ticket will appear in the web browser view immediately after you click "Pause" on the mobile app:

You can save your progress at any time by clicking 'Save'. This allows you to switch to another Smart Form and return later to complete your work.

Once the Smart Form is fully completed, you can click the downward-facing triangle next to 'Save' to access the 'Submit' option. Submitting the form finalizes it, preventing any further edits—whether through the mobile app or the web interface—after synchronization. It is recommended to submit Smart Forms only after the review process is complete and the CB is ready to make the certification decision.

To pause the audit, click the corresponding button located at the bottom left corner. This feature is recommended if you need to reopen the audit later on your mobile device due to unforeseen circumstances.

To fully close the audit on your mobile app, first click 'Finish', then select 'Finished'. After this step, no further edits can be made to the audit via the mobile application. It is recommended to use this functionality after the review process is complete and the CB is ready to make the certification decision.

After pausing or finalizing the audit, you must synchronize the mobile app to transfer all data—including NCs, images, and other inputs—to the web interface. To do this, ensure your device is connected to the internet and press the synchronization button.

Is the auditor able to add another product or PHU while conducting the audit offline via the mobile app?

Unfortunately, this will not be feasible, as the audit scope is required to be defined while connected to the online system.

Is it compulsory to use the mobile app?

No, you can perform the audit through the user web interface, the mobile app (which also works offline), or by integrating via an API.

How do the auditors access the mobile app? Where to download it from?

Instructions can be found here.

Mobile app Onboarding Instructions for Windows devices

Prerequisite: The user has a license key available and a user in the CertifierOS portal  

Note: Depending on the device and software version, the user experience may differ from the one described below. 

PREPROD (test) Environment 

  1. Install the desktop application file for testing in PREPROD environment. The application is available here: Osapiens.Operations_1.4.7.0_x86_x64.appxbundle 
  1. Download the installation file and follow the instructions presented on the screen 
  1. Note that the application needs to be installed directly to the device where the application is intended to be used 
  1. Once the application has been installed, open the application 
  1. Enter the license key and select “Activate Device” A black background with text and a key

Description automatically generated 
  1. In the next screen, select “Synchronize” so that organizational settings of your CB are imported 
  1. Enter the username and password of the user who will use the mobile application. The username and password are the same that are used to log in to the online portal for Certifier OS 
  1. The user should now see the audit overview screen and the different audits that have been assigned to the user 

LIVE Environment 

  1. Install the desktop application file for testing in PREPROD environment. The application is available here: Osapiens.Operations_1.4.7.0_x86_x64.appxbundle 
  1. Download the installation file and follow the instructions presented on the screen 
  1. Note that the application needs to be installed directly to the device where the application is intended to be used 
  1. Once the application has been installed, open the application 
  1. Enter the license key and select “Activate Device” A black background with text and a key

Description automatically generated 
  1. In the next screen, select “Synchronize” so that organizational settings of your CB are imported 
  1. Enter the username and password of the user who will use the mobile application. The username and password are the same that are used to log in to the online portal for Certifier OS 
  1. The user should now see the audit overview screen and the different audits that have been assigned to the user 
Mobile App Onboarding Instructions for Android Devices 

Prerequisite: The user has a license key available and a user in the CertifierOS portal 

Note: Depending on the Android device and software version, the user experience may differ from the one described below. 

PREPROD (test) Environment 

  1. Install the mobile application for testing in PREPROD environment. This is done via a dedicated installation file (apk file) which is available here: ServiceOS_1.4.7(270861)-PP.apk 
  1. Note that the file needs to be downloaded and installed directly to the device where the application is intended to be used 
  1. Once the application has been installed, open the application 
  2. Enter the license key and select “Activate Device”
    1. In the next screen, select “Synchronize” so that organizational settings of your CB are imported 
    1. Enter the username and password of the user who will use the mobile application. The username and password are the same that are used to log in to the online portal for Certifier OS 
    1. The user should now see the audit overview screen and the different audits that have been assigned to the user 

    LIVE Environment 

    1. Install the mobile application for testing in LIVE environment. The application is available in the Google Play store: osapiens HUB for Maintenance – Google Play  
    1. Note that the application needs to be installed directly to the device where the application is intended to be used 
    1. Once the application has been installed, open the application 
    2. Enter the license key and select “Activate Device”
    1. In the next screen, select “Synchronize” so that organizational settings of your CB are imported 
    1. Enter the username and password of the user who will use the mobile application. The username and password are the same that are used to log in to the online portal for Certifier OS 
    1. The user should now see the audit overview screen and the different audits that have been assigned to the user 
    Is there a possibility to download smart forms/checklists, work offline and then upload them to the CertifierOS?

    No, but there is a possibility of using an offline mobile application (available for Android Windows and iOS) and synchronising the audits/work orders with the online GLOBALG.A.P. IT Platform.

    Please note that Apple computers are not supported. The mobile app is working only on iPhones and iPads

    Why generate Multiple License Keys for a Single User?

    Please note that each license key is valid for a single use only. If a mobile application user intends to operate the app on multiple devices (e.g., one Android and one Windows device), they must be provided with a separate license key for each device.

    The assigned audit information will nevertheless be synchronized across the devices for this single user. 

    How to generate License Keys for Multiple Users?
    1. Log in to the online portal at: PREPROD osapiens Portal - Login (for the PREPROD/test environment) and
      at: https://prod.osapiens.cloud/portal (for the LIVE environment)
    1. In the left-hand navigation menu, go to Administration -> Devices
    1. Click on “Create multiple licenses” (available from the dropdown menu): 
    1. Select the number of licenses needed 
    1. Select your organization (CB)
    1. Click “Save” to complete the process 
    1. The “Device Management” screen will now show the available licenses in your organization  
    1. You will need to distribute the license keys generated to the mobile application users
    1. Once the user has used the license key on their device, the “Last Logged In User” column will be populated with the username of that user and the license key is associated with that user. 

    How to generate License Keys for the mobile app for a Single User?

    To use the CertifierOS mobile application, each user needs to be assigned with a license key. GLOBALG.A.P. certification bodies can generate the license keys themselves by following these instructions. 

    1. Log in to the online portal at: PREPROD osapiens Portal - Login (for the PREPROD/test environment) and
      at: https://prod.osapiens.cloud/portal (for the LIVE environment) 
    1. In the left-hand navigation menu, go to Administration -> Devices 
    1. Click on “Create single license”  
    1. Select the username of the CB user to whom the license should be given. Please note that the username is the same as the one the user uses to log in to the platform 
    1. Make sure that the “License status” is active 
    1. Select your organization (CB):
    1. Click “Save” to complete the process 
    1. A license key has now been assigned to the specific user. The user needs to use the license key when first logging into the mobile application 

    Find additional information here regarding onboarding the mobile app

    View all
    How to change the language in the web user interface?

    Go to your user, on the right-hand side, press on the three dots -> edit ->

    For now, if you select a language other than English, some text may still appear in English. Translation will be completed gradually. Thank you for your patience.

    Can a CB make an excel template for P&Cs in the native language?

    You can make an excel but you won't be able to upload it to the system.

    In which languages is the checklist currently available?

    Currently the checklist is available only in the English language.

    Will the system become available in other languages?

    The user interface is available in English, Spanish, French, German, Portuguese and Dutch.

    Please note that some parts of the interface are only available in English for the time being. The remaining translations will be added soon.

    You can select the desired language via the user profile:

    View all
    What is the charge-triggering point in the new GLOBALG.A.P. IT Platform?

    Fees are triggered by CertifierOS when the certificate is issued. (The same applies with an extension.) 

    This information becomes visible in CB AT at the end of each month.

    Will the registration fees on the new GLOBALG.A.P. IT Platform be determined based on the maximum hectares and number of growing cycles?

    The registration fee for plants is calculated based on the area registered under first harvest for each crop. Any area that is used more than once in an annual certificate validity (certification cycle), for the cultivation of the same product only, shall be registered as further harvest. Areas registered under further harvest of the same product, are not subject to additional registration fees. Product quantity changes during the validity of a certificate may also result in changes of the registration fee.

    Where can we see the billing month to month?

    You can see the billing information in CB-AT under the Invoicing tab.

    Users will be able to view their monthly invoices under the Invoicing tab, as highlighted in the screenshot below.

    To download invoicing details as an Excel file, please click the Download button.

    Note: The screenshot provided is for reference only and was originally designed for VS certificates (as indicated in the disclaimer). However, a similar invoicing portal will be implemented for CertifierOS.

    The Invoicing portal for the new IT platform is currently under development and will be made available soon.

    How will the registration fee be charged in case a producer was registered in the Database, but the audit will be conducted in November?

    Registration fees apply to each individual producer and to each producer group member. They will be charged either from the old system or from the new platform.

    View all
    hello world!