APEC Regulatory Harmonization Steering Committee (RHSC)
Results
Procedural document
IMDRF/MC/N2
Procedural document: IMDRF/MC/N2
Published date
Procedural document
IMDRF/MC/N1
Procedural document: IMDRF/MC/N1 FINAL:2024 (Edition 7)
Published date
Procedural document
IMDRF/MC/N83 FINAL: 2024
Slide Template (MS PowerPoint) to assist in the development of presentations by Regulatory Authorities making IMDRF Membership Applications
Published date
Procedural document
FOR GUIDANCE ONLY - IMDRF/MC/N69 FINAL:2023 (Edition 8)
FOR GUIDANCE ONLY: IMDRF/MC/N69 FINAL:2023 (Edition 8)
Published date
Procedural document
IMDRF/MC/N75 FINAL:2023 (Edition 2)
IMDRF Working Group Membership Application Form
Published date
Procedural document
IMDRF/MC/N76
Strategic Principles for IMDRF trainings (N76)
Published date
Procedural document
IMDRF/MC/N39
The strategic plan outlines the mission, objectives and priorities of the International Medical Device Regulators Forum (IMDRF).
Published date
Consultation
IMDRF terminologies for categorized Adverse Event Reporting (AER): terms, terminology structure and codes (Edition 4) - Annex А (Edition 3), G, Adverse Event Terminology Working Group, Coordinator Hiroshi Ishikawa, Closed 10 September 2019.
Consultation
IMDRF Terminologies for Categorized Adverse Event Reporting (AER): terms, terminology structure and codes - Annex B, Adverse Event Terminology Working Group, Coordinator Hiroshi Ishikawa - Pharmaceuticals and Medical Devices Agency (PMDA), Japan, Closed Wednesday, 31 May 2017.
Consultation
IMDRF Terminologies for Categorized Adverse Event Reporting (AER): terms, terminology structure and codes, Adverse Event Terminology Working Group, Coordinator Hiroshi Ishikawa, Pharmaceuticals and Medical Devices Agency (PMDA), Japan, Closed Friday, 12 October 2018.