Good Regulatory Review Practices (GRRP)
- IMDRF/GRRP WG/N40 FINAL:2024 (Edition 2) Competence, Training, and Conduct Requirements for Regulatory Reviewers
- IMDRF/GRRP WG/N47 FINAL:2024 (Edition 2) Essential Principles of Safety and Performance of Medical Devices and IVD Medical Devices
- IMDRF/GRRP WG/N52 FINAL:2024 (Edition 2) Principles of Labelling for Medical Devices and IVD Medical Devices
- IMDRF/GRRP WG/N59 FINAL:2024 (Edition 2) Requirements for Regulatory Authority Recognition of Conformity Assessment Bodies Conducting Medical Device Regulatory Reviews
- IMDRF/GRRP WG/N61 FINAL:2024 (Edition 2) Regulatory Authority Assessment Method for Recognition and Surveillance of Conformity Assessment Bodies Conducting Medical Device Regulatory Reviews
- IMDRF/GRRP WG/N63 FINAL:2024 (Edition 2) Competence and Training Requirements for Regulatory Authority Assessors of Conformity Assessment Bodies Conducting Medical Device Regulatory Reviews
- IMDRF/GRRP WG/N66 FINAL:2024 (Edition 2) Assessment and Decision Process for the Recognition of a Conformity Assessment Body Conducting Medical Device Regulatory Reviews
- IMDRF/GRRP WG/N71 FINAL:2024 (Edition 2) Medical Device Regulatory Review Report: Guidance Regarding Information to be Included
- IMDRF/GRRP WG/N89 Playbook for Medical Device Regulatory Reliance Programs