FDA 2018.06.25 医薬品査察の遅延、拒否、制限、拒絶に相当する状況についてのガイダンス COPY TITLE&URL 医薬品査察の遅延、拒否、制限、拒絶に相当する状況についてのガイダンス ]]> Tweet Share Hatena Pocket RSS feedly Pin it 設計移管とは Previous post Applying Human Factors and Usability Engineering to Medical Devices(邦訳版) Next post
FDA 2018.06.24 Guidance for Industry, Third Parties and Food and Drug Administration Staff – Medical Device ISO 13485:2003 Voluntary Audit Report Submission Pilot Program (FDA 20123.19)
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