This content is current only at the time of printing. This document was printed on 28 January 2021. A current copy is located at https://apvma.gov.au/node/62206
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Proposed approval of the new active constituent cross-linked polyacrylamide hydrogel, and the registration of the product, Arthramid Vet
This consultation closed on 24 February 2020.
Consultation period:
28 January 2020 to 24 February 2020The APVMA is considering an application for the approval of the new active constituent, cross-linked polyacrylamide hydrogel, and the registration of the product, Arthramid Vet.
We invite comment from 28 January 2020 to 24 February 2020 on whether the application for registration of the product and approval of the active constituent should be granted.
The APVMA is able to consider comments relating to the legislative grounds for registration, including:
- chemistry and manufacture
- occupational health and safety
- public health
- safety and first aid
- environmental safety
- efficacy and target animal safety
For more information, see page 34 of Gazette No. 2, 28 January 2020.
Please send your written submission by email or post to:
Contact Officer
Australian Pesticides and Veterinary Medicines Authority
GPO Box 3262
Sydney NSW 2001
Phone: +61 2 6770 2300
Email: enquiries@apvma.gov.au