Best Practices for Compliance with FDA 21CFR1040 - 2016

  • 26 Apr 2016
  • Webinar

Description

Topics
  • Develop and document the test results in a meaningful report
  • Develop and document a quality checklist that represents the safety features of the tested system
  • Learn FDA requirements on GMP training for the tested system
Who should Attend
  • Laser Safety Officers
  • Laser System Manufacturers
  • Laser Importers
  • Laser Integrators
  • Engineering Managers
  • Purchasers of Laser Systems
  • Contact Officials
  • Safety Managers
  • Speaker Profile

Past Events

Important

Please, check "Best Practices for Compliance with FDA 21CFR1040" official website for possible changes, before making any traveling arrangements

Event Categories

Government & Global Issues: Law & Regulations
Health & Medicine: Medical device, Medical technology
Technology: Equipment & machinery, Optics

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