Zdrowie i gospodarka · 24/07/1995

FDA Releases Working Draft of Revised CGMP Regulation for Medical Devices

The Food and Drug Administration (FDA) has made available a working draft of its revised Current Good Manufacturing Practice (CGMP) regulation for medical devices, which includes requirements for designing, manufacturing, and servicing medical devices intended for human use, and invites public comments and attendance at a public meeting to be held on the draft.