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2018.06.25

設計移管とは

2018.06.25

FDA対応設計アウトプットの要点

2018.06.24

お役立ち翻訳（ANNEX 11）

Medical Device Software

2018.06.24

医療機器に搭載するソフトウェアの品質保証

2018.06.24

品質保証部門の力量向上・支援サービス

Computer System Implementation

2018.06.24

品質イベント管理システムとは

Computer System Implementation

2018.06.24

FDA対応PLM＊1 構築の留意点

2018.06.24

MS-Excelに関するワーニングレター

2018.06.24

ソフトウェアに関するワーニングレター

Pharmaceutical Affairs Law

2018.06.24

医療機器の特性を踏まえた規制の構築

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Informative
- Pharmaceutical
- Medical Device
FDA QSR (21 CFR Part 820)
User Account

Informative
- Pharmaceutical
- Medical Device
FDA QSR (21 CFR Part 820)
User Account

Informative
- Pharmaceutical
- Medical Device
FDA QSR (21 CFR Part 820)
User Account

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