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June 12 2024
Wednesday 15:05
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【IEC-62304対応】ソフトウェア開発手順書一式
451000 (yen)
ecompliance
医療機器企業におけるCSV実践セミナー
66000 (yen)
ecompliance
[書籍] 技術移転(試験法・製法)実施手順と同等性確保ー各ス
60500 (yen)
ecompliance
【IEC-62304対応】ソフトウェア単体テスト手順書
33000 (yen)
ecompliance
【GMP省令対応】職員の衛生管理規程・手順書・様式
66000 (yen)
ecompliance
[書籍] <テクニカルトレンドレポート> シリーズ1[FOWLP・F
22000 (yen)
ecompliance
欧州医療機器規則(MDR)最新情報と医療機器の臨床評価の�
47300 (yen)
ecompliance
具体的な事例で学ぶGMP実践
44000 (yen)
ecompliance
【コンピュータ化システム適正管理ガイドライン対応】シ�
66000 (yen)
ecompliance
生物学的安全性評価の基本的考え方と運用セミナー
44000 (yen)
ecompliance
[書籍] 承認申請におけるCTD-Q作成での日本特有の要求事項対
44000 (yen)
ecompliance
[書籍] 半導体製造プロセスを支える洗浄・クリーン化・汚�
33000 (yen)
ecompliance
【GMP省令対応】自己点検規程・手順書・様式
66000 (yen)
ecompliance
【MDSAP適合性チェックリスト】製造及びサービス管理(CH6)
33000 (yen)
ecompliance
FDA QMSR発出のインパクト
22000 (yen)
ecompliance
【2021年度改正QMS省令対応】識別規程・手順書
55000 (yen)
ecompliance
【GMP省令対応】原材料の検査規程
33000 (yen)
ecompliance
[書籍] 医薬品開発を例にしたコンメンタール(逐条解説)研究
14960 (yen)
ecompliance
【2021年度改正QMS省令対応】トレーサビリティ管理規程・手�
55000 (yen)
ecompliance
【GMP省令対応】不適合品管理規程・手順書・様式
66000 (yen)
ecompliance
【ISO-13485対応】作業環境管理手順書
33000 (yen)
ecompliance
【FDA CFR 820 QMSR対応】プロセスバリデーションひな形セット
121000 (yen)
ecompliance
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