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Zdrowie i gospodarka · 14/02/2012

FDA Seeks Public Comment on Proposed Medical Device Reporting Rule

The Food and Drug Administration (FDA) is seeking public comment on a proposed rule requiring medical device manufacturers, importers, and distributors to report certain information. The proposed rule is part of the Paperwork Reduction Act of 1995 and aims to improve the reporting of medical device incidents.

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