Regulatory Directive: Master Product/Master Copy Registration Process (French, HTML)

Regulatory Directive: Master Product/Master Copy Registration Process: French HTML file. From Health Canada, updated Jul 2021. View metadata, licence and the direct download on CanQuery.

Format

HTML

Access

Original download only

Publisher-reported update

2021-07-30

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.

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