A detailed documented system is required showing that all Places of First Arrival (POFA) have the arrangements, facilities and systems in place to effectively manage risks associated with the importation of risk goods.

This application form is to be used for the purposes of applying for approval, (a) for a transitional facility &/or containment facility, under the Biosecurity Act 1993.

Use this form to apply for approval to conduct research on an ACVM product.

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

Must be completed by each importer/distributor of HGPs in NZ under the AVCM Act 1997

Use this form to declare that your imported product will not be used as an agricultural compound as defined by the ACVM Act.

A QCP is a document that outlines procedures relating to the manufacture, storage, testing and export of dairy quota product to a designated market. Dairy quota product must be processed and exported in accordance with an approved QCP before an export approval can be issued. It’s designed to ensure dairy quota product complies with the access requirements of a designated market.