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Shuren Highlights CDRH Actions To Ease Trial Burdens On Capitol Hill

CDRH Director Jeffrey Shuren participated in the first roundtable of a newly launched House Energy and Commerce Committee initiative to accelerate drug and device development. He emphasized the device center’s recent proposals to minimize pre-market data collection with postmarket controls, and supported the promise of clinical trial networks.

Jeffrey Shuren emphasized recent efforts by FDA’s device center to reduce premarket clinical trial burdens in return for strong postmarket controls during the May 6 inaugural roundtable of the House Energy and Commerce Committee’s “21st Century Cures” initiative.

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