新規に質問を投稿する場合はこちら。 Advance Filter by Select filter byFeaturedSolvedUnsolved Status AllProcessingHoldSolved Categories Select a category 製薬規制全般(2) - GLP(2) - GCP() - GMP() - cGMP() - PIC/S GMP() CSV(3)ER/ES(2)General(0)医療機器規制全般(43) - MDR(43) - QMSR() - ISO 10993() その他(13)データインテグリティ(3) Order by Select orderbyDateTitleRandomComment CountAnswer CountView CountVote Count Order Descending Ascending Per page 10 20 30 40 50 60 70 80 90 100 0Vote 1Answer 861View 原薬製造業者に対するFDA査察の基準 Solved Asked by Masayuki 11月 06, 2024 Last replied by ecompliance 0Vote 1Answer 1011View スプレッドシートとOffice 365 Solved Asked by Minami Koji 11月 01, 2024 Last replied by ecompliance 0Vote 1Answer 734View 欧州電池規則について Asked by hiroki kato 11月 01, 2024 Last replied by ecompliance 0Vote 1Answer 909View PDFでの文書確認について Solved Asked by ナミキ 11月 01, 2024 Last replied by ecompliance 0Vote 1Answer 686View ISO 10993-1 Asked by ecompliance 11月 01, 2024 Last replied by ecompliance 0Vote 1Answer 671View エンドポイント試験の省略について（ISO 10993-1） Asked by ecompliance 11月 01, 2024 Last replied by ecompliance 0Vote 1Answer 1036View MEDDEVとMDCG Asked by ecompliance 10月 31, 2024 Last replied by ecompliance 0Vote 1Answer 955View 生物学的安全性評価（JIS T 0993-1）について Asked by ecompliance 11月 01, 2024 Last replied by ecompliance 0Vote 1Answer 682View MDRにおける同等性評価 Asked by ecompliance 11月 01, 2024 Last replied by ecompliance « 前へ 1 … 7 8 9 新規に質問を投稿する場合はこちら。
