Regulatory Directive: Master Product/Master Copy Registration Process

Regulatory Directive: Master Product/Master Copy Registration Process is an open dataset from Health Canada with 2 files (HTML); catalogue record updated 2021-07-30. On CanQuery you can follow the original downloads. Files are available in English and French.

The Master Copy Registration Process has been put in place to streamline product registration procedures in the interests of improving operating efficiency and service to clients. Once a registered product is granted Master Product status, it may be used as a precedent for the registration of subsequent Master Copies. Master Product status may be requested in the initial submission for registration or, through amending a currently registered product.

Publisher

Health Canada

Resources

2

Catalogue metadata updated

2021-07-30