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How to Audit API Manufacturers

 
  January 21, 2009  
     
 
Pharma Training Services, Radisson SAS, Cork, Ireland
2009/04/30


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
 
 
Organized by: PharmaTraining Services
Invited Speakers: To be advised
 
Deadline for Abstracts: Not applicable
 
Registration: Please see weblink
E-mail: judy@pharmatrainingservices.com
 
   
 
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