2022.02.08 Part11 FDA CDER「Use of Electronic Records and Electronic Signatures in Clinical Investigations Under 21 CFR Part 11 – Questions and Answers」
FDA 2018.06.24 UDI Rule and Guidances, Training, Resources, and Dockets COPY TITLE&URL UDI Rule and Guidances, Training, Resources, and Dockets ]]> Tweet Share Hatena Pocket RSS feedly Pin it UDI(個体識別、Unique Device Identification) Previous post UDI Basics Next post
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