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Date: 9th February, 2010

Location: On-line, USA

Summary:
Pharmaceutical - Web Seminar

This webinar will provide a summary of best practices for steam sterilization validation drawing upon the experience gained over 30 years of work. Mr. Agalloco was chairman of PDA’s Rask Force for the Revision of TM#1 – Validation of Steam Sterilization in Autoclaves. He is currently the lead author responsible for updating USP Sterilization and Sterility Assurance for Compendial Articles chapter. The following areas will be addressed:

• Development of scientifically sound and compliant validation protocols
  


• Defining 'worst case' conditions and effective bracketing / matrixing of activities
  


• The difference between parts and terminal sterilization validation expectations
  


• Executing validation studies in an efficient manner
  


• Preparation of validation summary reports
  


• Maintaining regulatory compliance