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International GMPs: Complying with Requirements in the U.S., EU and Japan

Return to Your Job with a Detailed Matrix that Highlights the Differences in GMP Requirements in the U.S., EU and Japan!

  • 02/09/2009 - 02/10/2009

    Princeton, NJ

  • 02/23/2009 - 02/24/2009

    Toronto, Canada

  • 03/16/2009 - 03/17/2009

    San Francisco, CA

Who Should Attend

This course is intended for those who are involved with manufacturing operations and those who are responsible for ensuring compliance with international regulations. Professionals in the Pharmaceutical, Biotechnology and Medical Device industries should attend, including:

  • QA Specialists/Managers/Directors
  • Regulatory Affairs Specialists/Managers
  • Compliance Managers/Auditors
  • Global Affairs
  • Global Clinical Operations
  • Manufacturing Operations
  • Project Managers
  • Group Leaders
  • GMP Auditors/Trainers
  • Documentation Specialists/Managers
  • Validation Specialists/Managers
  • Laboratory Managers
  • Plant Managers
  • IT/IS Analysts or Engineers

Booking Options

Booking Options:

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