IMDRF Standards Checklist modified in scope of COVID-19
Posts tagged as “International Medical Device Regulators Forum – IMDRF”
Coronavirus Prompts IMDRF to Cancel 3 Meetings
IMDRF Final Documents – Clinical Evidence, Clinical Evaluation and Clinical Investigation
IMDRF terminologies for categorized Adverse Event Reporting (AER): terms, terminology structure and codes (Edition 4) – Annex А (Edition 3), G