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Medical Devices in the EU & US

10th June 2013

PLF Seminar with MHRA


This interdisciplinary seminar will bring together distinguished speakers from a variety of backgrounds, including lawyers, scientists, physicians and regulators to discuss this topic at a workshop subject to Chatham House rules.

Chaired by Sir Gordon Duff, Chairman, MHRA
Speakers include
John Wilkinson, Director of Devices, MHRA
Pamela Furman Forrest, King & Spalding, Washington DC, an expert on US Devices regulations & liability.

This event will cover both the regulatory differences in the US and EU, and explore how current concerns in the Medical Device sphere have been addressed by each system. There will also be an update on the reform at an EU level.

This is a Product Liability Forum event and attendance is by invitation only.

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