Basics of US Medical Device Regulation

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

The Basics of US Medical Device Regulation covers topics such as:

  • Post marketing
    • CAPA
    • QSR
    • Inspections
    • Reporting
    • Export for foreign markets
  • Clinical Trials
    • Other
    • IDE
    • Common problems in trial design and management
    • Export for trials

The Basics of US Medical Device Regulation brings together:

  • 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

Future Events

Basics of US Medical Device Regulation 2020

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