We’re improving our guidance material, tailoring it to the information you need to lodge the right application, with the right data and supporting evidence to meet APVMA criteria.
Whether you’re registering a new product or making a variation, you’ll have access to current and clear guidance for that application type before you enter our online services portal.
The following tailored guidance is available now. At the end of the process you’ll be able to start an application:
New product registrations
I want to register a new product with an existing active or new combination of approved actives
I want to register a product that is based on an existing registered reference product
I want to register a product and apply for the concurrent approval of a new source of active
Additional labels for a registered product
Variations to registered products
I want to vary my product to amend a restraint, contraindication, precaution or side effect statement (vet products only)
I want to vary a re-entry or handling instruction for my product
I want to vary my product to add a new crop, animal species or situation
I want to vary a product pack size
I want to vary my product to make a change to the product formulation—New
The tailored guidance materials are an alternative pathway to the existing decision tree, which is still available.
We’ll be gradually making more tailored guidance available for other common types of applications.
APVMA, 14 July 2020