Description
These guidelines interpret the requirements for good manufacturing practices (GMP) in Part C, Division 2 of the Regulations. Guidance documents like this one are meant to help industry and health care professionals understand how to comply with regulations. They also provide guidance to Health Canada staff, so that the rules are enforced in a fair, consistent and effective way across Canada.
Resources
| Name | Format | Description | Link |
|---|---|---|---|
| Good manufacturing practices guide for drug products (GUI-0001) - Summary | HTML | Open resource | |
| Good manufacturing practices guide for drug products (GUI-0001) - Summary | HTML | Open resource |