This one day seminar is aimed at QA staff in drug products manufacturers and especially their QPs who have specific responsibilities under directive 2004/27/EC. Participants will learn about the legislators' perspectives and the key differences between APIs and products, which lead to different audit techniques and thought processes when auditing API manufacturers
How to Audit API Manufacturers
13 November 2008, London, United Kingdom
Introduction
Venue
The Window Conference Centre
The Window Conference Centre, 13 Windsor Street, London, N1 8QG, United Kingdom
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Organised by
PharmaTraining Services
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