2020.02.23 EUにおける医療機器規制(MDR/IVDR) Guidance on Article 15 of the Medical Device Regulation (MDR) and in vitro Diagnostic Device Regulation (IVDR) regarding a 'person responsible for regulatory compliance'(PRRC)
Pharmaceutical 2019.01.21 Annex 15: Qualification and Validation(邦訳) COPY TITLE&URL Annex15_Qualification_and_Validation_Jダウンロード https://youtu.be/Fbai3zbopvQ ]]>
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