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Zdrowie i gospodarka · 02/04/2001

FDA Releases Draft Guidance for Biomaterials Access Assurance Act of 1998

The FDA is releasing a draft guidance outlining the procedures for petitioning for a declaration that a biomaterials supplier should have registered as a medical device establishment or listed its products with FDA, in accordance with the Biomaterials Access Assurance Act of 1998.

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