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(0)医療機器規制全般(14) - MDR(14) - QMSR() - ISO 10993() その他(8)データインテグリティ(2) 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 345View 欧州電池規則について Asked by hiroki kato 11月 01, 2024 Last replied by ecompliance 0Vote 1Answer 487View 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 315View ISO 10993-1 Asked by ecompliance 11月 01, 2024 Last replied by ecompliance 0Vote 1Answer 312View 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 340View MEDDEVとMDCG Asked by ecompliance 10月 31, 2024 Last replied by ecompliance 0Vote 1Answer 392View 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 329View MDRにおける同等性評価 Asked by ecompliance 11月 01, 2024 Last replied by ecompliance « 前へ 1 2 3 4 新規に質問を投稿する場合はこちら。
