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Corrective & Preventative Action (CAPA) & Out of Specification (OOS)

 
  November 07, 2008  
     
 
Centre for Applied Training and Development, London, UK
2009-03-16 & 2009-03-17


This two-day training course will guide and develop your understanding of: ·     Regulatory Requirements for CAPAs and OOS Investigations·     Secure Strategies for Compliance     ·     How to Maximize Benefits from CAPAs and OOS Investigations ·     How to Manage Typical Issues that Arise Both FDA and European Regulators expect pharmaceutical products manufacturers to have in place a system for CAPA to correct process deficiencies and maximise process improvement.  In addition, manufacturers must have a secure system for management of Out of Specification Results (Non-Conformances) to ensure that all product on the market is safe and meets its registration requirements.
 
 
Organized by: Centre for Applied Training and Development
Invited Speakers:

info@catdglobal.com

 
Deadline for Abstracts: n/a
 
Registration: Please refer to the register tab on the CATD website (www.catdglobal.com) or click on the title of the course on the conferences/meeting or home page to register on line.If you have any problem registering please do not hesitate to contact us at info@catdglobal.com or call us at + 44 (0) 20 8485 1234 or fax us at + 44 (0) 20 8485 1234
E-mail: info@catdglobal.com
 
   
 
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