Technical document IMDRF/PMD WG/N58:2023 (Edition 2) Personalized Medical Devices - Regulatory Pathways 14 September 2023
Information document IMDRF/MC/N78 FINAL:2023 IMDRF Strategic Plan 2021-2025 - Progress Report Card 8 May 2023
Information document IMDRF/MC/N77 White Paper - 23rd IMDRF Session Joint Workshop by IMDRF – DITTA and GMTA on the importance of post-market related activities 24 April 2023
Technical document IMDRF/CYBER WG/N73 Principles and Practices for Software Bill of Materials for Medical Device Cybersecurity 13 April 2023
Technical document IMDRF/PMD WG/N74 Personalized Medical Devices – Production Verification and Validation 11 April 2023
Technical document IMDRF/CYBER WG/N70 Principles and Practices for the Cybersecurity of Legacy Medical Devices 11 April 2023
Technical document IMDRF/NCAR WG/N14 Medical Devices: Post-Market Surveillance: National Competent Authority Report Exchange Criteria and Report Form 11 April 2023
Technical document IMDRF/GRRP WG/N71 Medical Device Regulatory Review Report: Guidance Regarding Information to be Included 7 February 2023