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)医療機器規制全般(23) - MDR(23) - QMSR() - ISO 10993() その他(12)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 389View 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 666View 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 418View 欧州電池規則について Asked by hiroki kato 11月 01, 2024 Last replied by ecompliance 0Vote 1Answer 602View 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 381View ISO 10993-1 Asked by ecompliance 11月 01, 2024 Last replied by ecompliance 0Vote 1Answer 393View 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 481View MEDDEVとMDCG Asked by ecompliance 10月 31, 2024 Last replied by ecompliance 0Vote 1Answer 497View 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 400View MDRにおける同等性評価 Asked by ecompliance 11月 01, 2024 Last replied by ecompliance « 前へ 1 … 4 5 6 新規に質問を投稿する場合はこちら。
