This content is current only at the time of printing. This document was printed on 8 September 2020. A current copy is located at http://www.gitygostar.com/taxonomy/term/18206
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I want to vary my product to alter the shelf life/expiry date, in-use shelf life and/or storage conditions
Applications to vary the shelf life details or storage conditions for registered products may be made via:
- Item 12: No data of a technical nature is required. This type of application is used when risks are equivalent to a registered product not subject to data protection
- Item 14: Technical modular application. All applications not meeting the requirements of Item 12.
Which application form do you need?
Specific information on completing this application form is provided below. Once you are familiar with the content you can proceed to ‘Start an application’ at the button below.
All veterinary chemical products are date-controlled. Shelf life must be recorded, and product labels must contain information on the storage conditions and expiry date of the product. Some veterinary chemical products also have an in-use shelf life, which is the shelf life of the product after first broaching the container.
Is a technical assessment required for my proposed variation?
For a variation to be processed without a technical assessment (Item 12), all risk areas must be supported by solely referencing another registered product (reference product). Applicants seeking to rely on a reference product should explain the reasons why the reference product supports the variation. This should include how the risks are equivalent between the two products including:
- similarity in instructions for use (animals, claims, dose, route of administration)
- the active constituent and its concentration
- the formulation type.
Limits on use (data protection)
Where there are limits on use of information on the reference product written consent from the authorising party is required when access to the information is necessary to determine the application.
Where the reference product does not fully support all risk areas or the product is subject to limits on use and additional data is being provided to satisfy the safety, efficacy or trade criteria these applications should be lodged as Item 14 applications.
Most product shelf life variations are likely to be made as Item 14 applications.