APEC Regulatory Harmonization Steering Committee (RHSC)
Results
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The International Medical Device Regulators Forum (IMDRF) aims to accelerate international medical device regulatory harmonization and convergence.
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Medical device safety information published by the National Competent Authority Report (NCAR) Exchange Members.
Working group
Harmonize the regulatory requirements for medical devices that are intended for a particular individual, considering unique characteristics and risks associated with each type of device.
Consultation
Clinical Evidence for IVD Medical Devices – Definitions and Principles of Performance Evaluation
Working group
A working group on Clinical evidence for in vitro diagnostic (IVD) medical devices
Consultation
Definitions for Personalized Medical Devices, Personalized Medical Devices (PMD) Working Group, Coordinator Tracey Duffy, Closed 24 May 2018.
Consultation
Personalized Medical Devices - Regulatory Pathways, Personalized Medical Devices (PMD) Working Group, Coordinator Tracey Duffy, Closed 24 July 2019.
Consultation
Personalized Medical Devices Regulatory Pathways - Personalized Medical Devices
Consultation
Personalized Medical Devices Production Verification and Validation, Personalized Medical Devices
Consultation
Principles and Practices for the Cybersecurity of Legacy Medical Devices, Medical Device Cybersecurity Guide, Coordinator Dr Aftin Ross, Closes 3 July 2022