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How to Audit API Manufacturers

30 April 2009, Cork, Ireland


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

Useful links

Venue
Radisson SAS Hotel

Radisson SAS Hotel, Cork, Ireland

Organised by
Pharma Training Services
Contact information
Ms Judy Callanan
Pharma Training Services, Biocity Nottingham, Pennyfoot Street, Nottingham, NG1 1GF, United Kingdom
+44 20 7193 7703
Contact us by email

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