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FDANonrulemakingFDA-2017-D-2802

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CMC Postapproval Manufacturing Changes for Specified Biological Products To Be Documented in Annual Reports

1 organizations filed 1 public comment on CMC Postapproval Manufacturing Changes for Specified Biological Products To Be Documented in Annual Reports, at the Food and Drug Administration. The comment window closed 3213d ago.

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Who Commented on CMC Postapproval Manufacturing Changes for Specified Biological Products To Be Documented in Annual Reports (FDA-2017-D-2802) | OpenPolis