Good manufacturing practices guide for drug products (GUI-0001) - Summary
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.
- Publisher - Current Organization Name: Health Canada
- Licence: Open Government Licence - Canada
Data and Resources
-
Good manufacturing practices guide for drug products (GUI-0001) - SummaryHTMLEnglish publication HTML
-
Good manufacturing practices guide for drug products (GUI-0001) - SummaryHTMLFrench publication HTML