ESC 365 - Marketing of medical devices in the US & Europe: focus on regulatory requirements and patient access

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Marketing of medical devices in the US & Europe: focus on regulatory requirements and patient access

Session: Approval processes for medical devices - Understanding clinical and regulatory perspectives - Spotlight on coronary stents

Topic: Miscellaneous

Speaker: Professor R. Waksman (Washington, DC, US)

Event: ESC Congress 2017

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About the speaker

Professor Ron Waksman

Washington Hospital Center & Medstar Health, Washington, DC (United States of America)

3 presentations

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5 more presentations in this session

The regulatory landscape in Europe: challenges and opportunities of the new EU Medical Devices Regulation

Speaker: Professor A. Fraser (Cardiff, GB)

Developing device-specific common standards in Europe. The regulators' perspective

Speaker: Mr C. Griesinger (Ispra, IT)

Clinical evaluation of coronary stents and bio-resorbable stents: ESC/EAPCI engagement with the EU regulatory system

Speaker: Professor R. Byrne (Dublin, IE)

EU cooperation on HTA: where are we and where do we want to go

Speaker: Professor P. Szymanski (Warszawa, PL)

Panel discussion: device regulation

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Approval processes for medical devices - Understanding clinical and regulatory perspectives - Spotlight on coronary stents

Speakers: Professor R. Waksman, Professor A. Fraser, Mr C. Griesinger, Professor R. Byrne, Professor P. Szymanski

About the event

ESC Congress 2017

26 August - 30 August 2017

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