Thursday, 15 May 2014

EU GMP Annex 15 Revisions: Improving Qualification and Validation

Validation and qualification form an important part of the quality system in the pharmaceutical sector and can be defined in different ways. Tim Sandle, Head of Microbiology, BPL, UK discusses some standard definitions from a Good Manufacturing Practice (GMP) perspective.

The article can be viewed on the CleanroomTechnology website here.

Posted by Tim Sandle