Basics of US Medical Device Regulation 2015

  • 17-18 Dec 2015
  • DoubleTree by Hilton Hotel San Francisco Airport, Burlingame, CA, United States

Description

The Basics of US Medical Device Regulation 2015 is dedicated to basics of US Medical Device Regulation.

Topics
  • Post marketing
    • CAPA
    • QSR
    • Inspections
    • Reporting
    • Export for foreign markets
  • Clinical Trials
    • Other
    • IDE
    • Common problems in trial design and management
    • Export for trials
Who should Attend
  • People who are Interested in Starting a Company to Sell Health-related Products
  • People who are Working in non Regulatory or QA Areas of Medical Device Companies
  • People who are Interested in Selling Medical Devices
  • People who are Interested in financing a Health Care Company

Past Events

Important

Please, check "Basics of US Medical Device Regulation" official website for possible changes, before making any traveling arrangements

Event Categories

Government & Global Issues: Law & Regulations
Health & Medicine: Medical device

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