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(32) - MDR(32) - 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 60View 承認前の原薬出荷 Asked by ノブ 9月 18, 2025 0Vote 1Answer 146View 医療機器を修理する場合の業許可 Asked by スガ 9月 04, 2025 0Vote 1Answer 130View 21 CFR Part 801- §801.109について Asked by K 8月 20, 2025 0Vote 1Answer 133View 21 CFR Part801の要件について Asked by ecompliance 8月 11, 2025 Last replied by ecompliance 0Vote 1Answer 130View QMS省令第45条について Asked by ecompliance 8月 11, 2025 Last replied by ecompliance 0Vote 0Answer 24View 非公開: Established Nameについて Asked by ecompliance 8月 02, 2025 0Vote 1Answer 173View アウトソースについて Asked by ecompliance 8月 06, 2025 Last replied by ecompliance 0Vote 1Answer 127View FD＆C Act. §352について Asked by ecompliance 8月 06, 2025 Last replied by ecompliance 0Vote 1Answer 184View 自社で製造した医療機器の修理品の検査、出荷許可等 Asked by ecompliance 8月 02, 2025 Last replied by ecompliance 0Vote 1Answer 184View 一般医療機器（クラスⅠ）の広告について Asked by ecompliance 8月 02, 2025 Last replied by ecompliance 1 2 3 … 8 次へ » 新規に質問を投稿する場合はこちら。
