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EU Regulatory Challenges for Medical Devices

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University of Washington Bothell – Beardslee Crossing

19128 112th Ave, Suite 102M/N

Bothell, WA 98011

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Join our 2-hour seminar on September 21st and learn how the new European Medical Device Regulation (MDR) will impact your business. Our industry experts will provide an overview about these changes, specific requirements for medical devices, and responsibilities of notified bodies.

Topics include:

  • New regulations
  • Clarification of existing process
  • Overview of CE Mark requirements
  • How to prepare for these changes

Speakers Include:

Antonio Dai-Pra- Market Access & Compliance Specialist, U.S. Commercial Service (Belgium Office)

Tembi Secrist- Director, Global Healthcare Team, U.S. Commercial Service

Julie Bennion, Life Science and Global Health Export Manager, Washington State Department of Commerce

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Location

University of Washington Bothell – Beardslee Crossing

19128 112th Ave, Suite 102M/N

Bothell, WA 98011

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