Food and Drug Administration FDA issued updated draft guidance, Electronic Systems, Electronic Records, and Electronic Signatures in Clinical Investigations–Questions and Answers. Draft Guidance revamps earlier recommendations from 2017 regarding requirements of 21 CFR Part 11.
On March 15, 2023, the U.S. Food and Drug Administration (“FDA”) issued updated draft guidance, Electronic Systems, Electronic Records, and Electronic Signatures in Clinical.
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/PRNewswire/ The "Additive Manufacturing by Technology by Printer Type by Material by Application by Component and by End-User - Global Opportunity Analysis.
/PRNewswire/ The "Additive Manufacturing by Technology by Printer Type by Material by Application by Component and by End-User - Global Opportunity Analysis.