2018.12.27 GMP省令改正(2021年)関連 サイトマスターファイル 製薬協・APAC(Asia Partnership Conference of Pharmaceutical Associations)での課題としてアジア規制当局、業界団体も調整して作成
FDA 2018.06.24 UDI Basics COPY TITLE&URL UDI Basics ]]> Tweet Share Hatena Pocket RSS feedly Pin it UDI Rule and Guidances, Training, Resources, and Dockets Previous post Guidance for Industry, Third Parties and Food and Drug Administration Staff - Medical Device ISO 13485:2003 Voluntary Audit Report Submission Pilot... Next post
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