Applying U.S. FDA Laws and Regulations to Each Phase of Total Product Life Cycle (TPLC) 2017

  • 25-26 May 2017
  • Hilton Garden Inn Philadelphia Center City, PA, United States

Description

Topics
  • An Overview of U.S. FDA Medical Device Regulation
  • Total Product Life Cycle and Your Medical Device
  • Premarket Notification - 510(k) and Premarket Approval (PMA)
  • Regulations for Design and Product Development
  • Readiness for FDA Facility Inspection
  • Regulations for Production & Process Control
Who should Attend
  • Regulatory Affairs - Associates and Specialists
  • Regulatory Affairs - VP, Director and Managers
  • Research & Development - Product Managers
  • Compliance Officers
  • Quality Assurance and Quality Engineers

Past Events

Important

Please, check "Applying U.S. FDA Laws and Regulations to Each Phase of Total Product Life Cycle (TPLC)" official website for possible changes, before making any traveling arrangements

Event Categories

Government & Global Issues: Law & Regulations
Health & Medicine: Healthcare, Medical device, Medical laboratories, Pharma
Industry: Food & Beverages
Technology: Biotechnology

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