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Guidance Documents/Guidance-Document/CMC Postapproval Manufacturing Changes To Be Documented in Annual Reports

CMC Postapproval Manufacturing Changes To Be Documented in Annual Reports

Detailed guidance document from FDA and regulatory agencies.

Document Details

Guidance Document

March 5, 2014

February 15, 2024

Center for Drug Evaluation and Research

67341cfe-8a48-4fc7-9817-6f9ed89768cf

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