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BioWorld - Thursday, January 22, 2026
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» Lack of detail plagues FDA’s opening salvo in Part 820 rewrite
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Lack of detail plagues FDA’s opening salvo in Part 820 rewrite
Feb. 22, 2022
By
Mark McCarty
The U.S. FDA has at last published what is nominally a draft rule for harmonization of the Quality System Regulation (QSR) with an international standard, ISO 13485, but the draft rule is conspicuous for the absence of specifics.
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