An Insider’s Perspective on the FDA Regulatory Process

FDA fellowship provides unique look “behind the scenes”

Madeleine Lovette

The U.S. Food and Drug Administration (FDA) is integral to ensuring that innovative orthopaedic drugs and devices reach musculoskeletal patients in a safe and timely manner. The FDA Center for Devices and Radiological Health (CDRH) Medical Device Fellowship Program (MDFP) provides opportunities for health professionals, including orthopaedic surgeons, to participate in the FDA regulatory process for medical devices.

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