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How to Audit API Manufacturers

13 November 2008, London, United Kingdom


Introduction
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
Venue
The Window Conference Centre

The Window Conference Centre, 13 Windsor Street, London, N1 8QG, United Kingdom

Organised by
PharmaTraining Services
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