Click on the tabs for more information about the status of each phase in the review process. For more information about how each phase is conducted, please read about the reconsideration process.
- RelatedConsultation paperConsultation summary paper
The Australian Pesticides and Veterinary Medicines Authority (APVMA) invites written submissions on the proposed changes to its fees and charges.
As the APVMA is a corporate Commonwealth Entity…
Overseas veterinary chemical product manufacturers need to provide acceptable evidence of Good Manufacturing Practice (GMP) to the Australian Pesticides and Veterinary Medicines Authority (APVMA) to import intermediate or finished…
- Permit applications for releasing out of specifications batches
The term out-of-specification (OOS) includes all test results that fall outside the specifications or acceptance criteria established at the time of registration of the product or during…
This document provides a list of contact details for Good Manufacturing Practice (GMP) auditors authorised by the Australian Pesticides and Veterinary Medicines Authority (APVMA). This document replaces the previous version published on 7 September…
- ContentsErratum notice – 1Agricultural chemical products and approved labels – 2Veterinary chemical products and approved labels – 18Approved active constituents – 23Amendments to the APVMA MRL Standard – 26Proposal to amend Schedule 20…
The Australian Pesticides and Veterinary Medicines Authority (APVMA) has opened consultation on proposed changes to its fees and levies which would come into effect on 1 July 2025.
Mr Scott Hansen APVMA CEO has encouraged stakeholders to…
During August and September 2024, the ABC has published a number of articles regarding the APVMA’s proposed regulatory decision on paraquat that make false or misleading claims.
The proposed regulatory decision is currently undergoing public…