EC Looking to Recommend Tougher Regulations on Medical Devices, More Member State Coordination

New changes are emerging from the French scandal involving breast implants. The European Commission (EC) will investigate whether or not to recommend

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Marc is dedicated to helping his clients navigate the complex world of FDA and USDA legislation. He represents FDA-regulated companies in the food, dietary supplement, beverage, cosmetic, medical device, and drug industries.

Marc is the author of two textbooks and a lecturer at Northeastern University. He is a member of the Washington State Bar Association and the D.C. Bar Association.

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