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Consultation - Guidance on the Control of Products and Services Obtained from Suppliers

Reminder: The current consultation regarding Guidance on the Control of Products and Services Obtained from Suppliers will close on 6 July, 2026.
25 June 2026

Consultation - Clinical Evidence for IVD Medical Devices – Definitions and Principles of Performance Evaluation

Reminder: The current consultation on IMDRF/CEIVD WG/N91 Draft: 2026 – Clinical Evidence for IVD Medical Devices: Definitions and Principles of Performance Evaluation will close on 5 May 2026.
23 April 2026

Voluntary Withdrawal of GHWP

Global Harmonization Working Party (GHWP) has voluntarily withdrawn from IMDRF.
8 July 2025

IMDRF Membership Forms now online

From May 2025, all IMDRF related forms will be available online from IMDRF’s Citizen Space site.
13 May 2025

Essential Principles of Safety and Performance - Workshop

Essential Principles of Safety and Performance of Medical Devices and IVD Medical Devices: Workshop record available fthrough GRRP Working Group
8 November 2024

IMDRF Working Group Updates available for review and feedback

IMDRF Working Group Updates to the 24th IMDRF MC Session available for review and feedback
8 September 2023

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14 July 2023

IMDRF Strategic Plan 2021-2025 - Progress Report Card

IMDRF Strategic Plan 2021-2025 - Progress Report Card
8 May 2023

Outcome statement available - 23rd IMDRF Meeting in Brussels, March 2023

23rd MC Meeting - Brussels Outcome Statement
28 April 2023

White Paper - 23rd IMDRF Session Joint Workshop by IMDRF – DITTA and GMTA: Importance of post-market related activities

White Paper - 23rd IMDRF Session Joint Workshop by IMDRF – DITTA and GMTA - Importance of post-market related activities
28 April 2023

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