2022.02.08 Part11 FDA CDER「Use of Electronic Records and Electronic Signatures in Clinical Investigations Under 21 CFR Part 11 – Questions and Answers」
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 2020.09.03 3 QSR関係(概論編) 21 CFR 820 QSR概要 COPY TITLE&URL https://www.youtube.com/watch?v=FtReaG_6Pvs 関連商品 [blogcard url=https://xn--2lwu4a.jp/qms-md/ title=”QMS(手順書)ひな形 医療機器関連” ] ]]> Tweet Share Hatena Pocket RSS feedly Pin it 1 QSR関係(製造管理編) プロセスコントロール Previous post 1 QSR関係(概論編) QMSの構築 Next post
FDA 2022.07.08 Department of Health and Human Services (HHS) criticizes the status of FDA’s overseas inspections
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