Guide to validation – drugs and supporting activities (GUI-0029) - Summary

This document is for anyone involved in the fabrication, packaging/labelling, testing, importation, distribution and wholesaling of drugs. It describes how to properly qualify and validate drug manufacturing processes, facilities, equipment, utilities and analytical methods.

Publisher
Health Canada
Resources
2
Catalogue metadata updated
2023-02-27

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HTML
File languages
English, French

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