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(1) - GLP(1) - GCP() - GMP() - cGMP() - PIC/S GMP() CSV(2)ER/ES(2)医療機器規制全般(16) - MDR(16) - QMSR() - ISO 10993() その他(10)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 379View 欧州電池規則について Asked by hiroki kato 11月 01, 2024 Last replied by ecompliance 0Vote 1Answer 546View 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 336View ISO 10993-1 Asked by ecompliance 11月 01, 2024 Last replied by ecompliance 0Vote 1Answer 347View 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 389View MEDDEVとMDCG Asked by ecompliance 10月 31, 2024 Last replied by ecompliance 0Vote 1Answer 445View 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 362View MDRにおける同等性評価 Asked by ecompliance 11月 01, 2024 Last replied by ecompliance « 前へ 1 … 3 4 5 新規に質問を投稿する場合はこちら。
