Post sponsored by

Source: New Zealand Ministry of Health

Parts 1 and 5 of this guideline are still to come.

Part 2: Information for New Zealand Manufacturers and Packers

This document provides prospective manufacturers and packers of medicinal cannabis products with relevant information about:

  • the Licence to Manufacture Medicines and the Licence to Pack Medicines under the Medicines Act 1981
  • how to comply with the New Zealand Code of Good Manufacturing Practice for Manufacture and Distribution of Therapeutic Goods.

Part 3: Guidance for a New Medicinal Cannabis Product Application

This document outlines how to make an application for a new medicinal cannabis product.

Part 4: Guidance for Applicants for a Medicinal Cannabis Licence

This document provides guidance on applying for a Medicinal Cannabis Licence under the Misuse of Drugs Act 1975 (the Act) and the Misuse of Drugs (Medicinal Cannabis) Regulations 2019 (the Regulations).

While we have made every effort here to explain the scope of the information that you need to provide in your application, it is your responsibility to understand your obligations under the Act and Regulations and provide true and accurate information in your application.

Please send all correspondence about your application to


Form A: Application for a Medicinal Cannabis Licence

Form D: Declaration of illicit seed and plants