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

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

 Send this completed form electronically to approvals@mpi.govt.nz
 Refer to the Privacy Act 1993 and Official Information Act 1982 notices at the end of this form regarding collection of information by the Ministry for Primary Industries.

Use this form to apply for renewal of your registered ACVM product.

Use this form to apply for any change to an ACVM registered product. See section 3 of this form for additional information required.

 Send this completed form electronically to CVM.ManufacturingandAssurance@mpi.govt.nz
 Along with the form, provide formal verification of this name change in the form of a letter or equivalent.
 Manufacturers who are Registrants: Please complete a C2 application (and update your Product Data Sheet) to ensure your name change is reflected in your ACVM product registrations that are impacted by this name change.
 Contract Manufacturers: Please advise the registrant of the ACVM registered products you manufacture of your company’s name change so they can complete a C2 application and update their approved Product Data Sheet and ensure their product registration remains current.
 Refer to the Privacy Act 1993 and Official Information Act 1982 notices at the end of this form regarding collection of information by the Ministry for Primary Industries.

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

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

Use this form to report an adverse event (unexpected effect) with an agricultural chemical

Use this form to report an adverse event (unexpected effect) with a VTA.

Use this form to report an adverse event (unexpected effect) with a veterinary medicine.

This form is for RTT organisations required to hold an MPI -approved operating plan under section 28 of the ACVM Act.

This form is for RTT organisations required to hold an MPI -approved operating plan under section 28 of the ACVM Act.

This form is for sellers/distributors of hormonal growth promotants (HGPs) required to hold an MPI -approved operating plan under section 28 of the ACVM Act

This form is for sellers of restricted veterinary medicines (RVMs) required to hold an MPI -approved operating plan under section 28 of the ACVM Act.