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  1. Medical Devices

Device Good Manufacturing Practice Advisory Committee

The Device Good Manufacturing Practice Advisory Committee (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.

Designated Federal Officer (DFO)
Serina A. Hunter-Thomas, M.S.A, B.S.N., R.N.
Office: (240) 402-5771
Cell: (240) 676-9852

Contact Information

FDA Advisory Committee Information Line
1-800-741-8138
(301-443-0572 in the Washington DC area)

Please call the Information Line for up-to-date information on this meeting.

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