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PROCESS VALIDATION
FOR PHARMACEUTICALS
& MEDICAL
DEVICES IN THE EU
& USA

Including practical workshop exercises

Conference Date: 23-24 Oct 2012
Conference Ref: M10-8012
Fee: £1260 + VAT
Venue: The Rembrandt Hotel, London

BENEFITS OF ATTENDING:

  • Understand the main differences between the process validation guidance from FDA (pharma), the draft from EMA (pharma) and the GHTF (medical device)
  • Discover a science and risk based approach to process validation
  • Experience the FDA process validation from design, process performance qualificiation to continued process verification
  • Discuss practical quality risk management and its application
  • Understand the importance of a supporting Quality System
  • Manage continual improvement and process optimisation
  • Take away significant business benefits

TO REGISTER FOR THIS EVENT CLICK HERE

If you have any queries please click here to contact Andrea James

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