Information document 1 April 2025 Medical Devices: Post-Market Surveillance: National Competent Authority Report Exchange Criteria and Report Form
Technical document 29 January 2025 Good machine learning practice for medical device development: Guiding principles
Technical document 29 January 2025 Characterization Considerations for Medical Device Software and Software-Specific Risk
Information document 30 October 2024 IMDRF 26th Session Workshop - White Paper on Developing a Regulatory Framework
Technical document 10 October 2024 Common Data Set for Adverse Event Data Exchange Between IMDRF Regulators
Outcome statement 4 October 2024 IMDRF 26th MC Meeting Seattle, Washington September 2024 - Outcome Statement
Technical document 25 June 2024 In Vitro Diagnostic Medical Device Regulatory Submission Table of Contents (IVD ToC)
Technical document 25 June 2024 Non-In Vitro Diagnostic Device Regulatory Submission Table of Contents (nIVD ToC)