Guidance Documents – Site licensing – Natural health products
- Good Manufacturing Practices
Date: March 2026 - version 4.0 - Site Licensing
Date: December 2015 - Version 3.0 This document outlines what a site licence is, when it is required, who must hold one, how to apply for one and how to change and renew one. It also describes the process applications go through when they reach the Natural and Non-prescription Health Products Directorate, and includes samples of all the necessary forms. It can be used as an aid to complete an effective site licence application, to provide clarity on how to maintain a valid site licence and to gain a better overall understanding of the site licensing process and regulations.
- Transition
Date: November 2003 This guidance document explains the provisions of Part 6 of the Natural Health Products Regulations, specifically sections 108 to 115, the provisions that govern the transition periods associated with the Regulations.