FDA delays draft rule for QSR/ISO 13485 harmonization

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The U.S. Food and Drug Administration (FDA) indicated that the long-anticipated proposed rule modernizing the Quality System Regulation (QSR) is now targeted for release in April 2020. This is the second delay in the agency's efforts to harmonize the framework regulating quality systems with the international consensus standard for medical device manufacture, ISO 13485:2016.

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