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)
FDA 2018.06.24 UDI Basics COPY TITLE&URL UDI Basics ]]> Tweet Share Hatena Pocket RSS feedly Pin it UDI Rule and Guidances, Training, Resources, and Dockets Previous post Guidance for Industry, Third Parties and Food and Drug Administration Staff - Medical Device ISO 13485:2003 Voluntary Audit Report Submission Pilot... Next post
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