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Zdrowie i gospodarka · 15/02/2013

FDA Announces Draft Guidance for Accreditation and Reaccreditation Process for Medical Device Review Firms

The Food and Drug Administration (FDA) has released a draft guidance outlining the criteria for accrediting and reaccrediting firms that review medical devices, with the goal of harmonizing processes with international regulating bodies.

Source: Federal Register — Food and Drug AdministrationOpen original release →