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How to Audit API Manufacturers

19 June 2009, 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

Who should attend
Supplier auditors for drug products manufacturers
QPs in manufacture of drug products
QA managers who support the QP / declaration
QC managers of drug products manufacturers
Production managers of drug products manufacturers.
Venue
Windows Conference Venue

Windows Conference Venue, Islington, London, United Kingdom

Organised by
Pharma Training Services
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