Must be completed by NZ manufacturers who carry out any step of manufacture of a veterinary medicine/vertebrate toxic agent registered under the ACVM Act 1997

Use this form to declare that ACVM products in your possession are for use only on animals you are accompanying.

Processing categories are used to aid in the registration of a Risk Management Programme or Amendment to a RMP as required under sections 20 and 25 of the Animal Products Act 1999 (APA) and for the purposes of review and/or update as required under section 26 of the APA.