Description
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.
Resources
| Name | Format | Description | Link |
|---|---|---|---|
| Guide to validation – drugs and supporting activities (GUI-0029) - Summary | HTML | Open resource | |
| Guide to validation – drugs and supporting activities (GUI-0029) - Summary | HTML | Open resource |