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FDA Seeks Experts on Medical Device Manufacturing Practices

11/09/2021

Respond by December 3, 2021

The U.S. Food and Drug Administration (FDA) is seeking five experts on medical device manufacturing practices to participate in FDA’s Device Good Manufacturing Practice Advisory Committee (DGMPAC) next year. This position would be the public expert advocate on this committee.

The DGMPAC reviews proposed regulations for good manufacturing practices governing the methods used in, and the facilities and controls used for, the manufacture, packing, storage, and installation of devices, and makes recommendations on the feasibility and reasonableness of the proposed regulations. Learn more on the FDA website.

Applicants will be required to submit their CV and go through a conflict of interest process. For more information, please contact Jarrod Collier [email protected] by December 3, 2021.

CONTACT

Jana Zabinski

Senior Director, Communications & Public Relations

Phone:
212.642.8901

Email:
[email protected]

Beth Goodbaum

Journalist/Communications Specialist

Phone:
212.642.4956

Email:
[email protected]