Zdrowie i gospodarka · 04/02/2003

FDA Establishes Public Docket for Medical Device User Fee and Modernization Act of 2002 Implementation

The Food and Drug Administration (FDA) is launching a public consultation process to gather feedback on the implementation of the Medical Device User Fee and Modernization Act of 2002 (MDUFMA), a law aimed at modernizing the regulatory framework for medical devices in the United States. The FDA invites all interested parties to share their views on the implementation of MDUFMA through a public docket.