MEDSAFE – Medical Device Adverse Event Reporting
Posts tagged as “Adverse Event Reporting – AER”
IMDRF terminologies for categorized Adverse Event Reporting (AER): terms, terminology structure and codes (Edition 4) – Annex А (Edition 3), G
June 25, 2022
News, opinions and insights about medical device regulations and standards
MEDSAFE – Medical Device Adverse Event Reporting
IMDRF terminologies for categorized Adverse Event Reporting (AER): terms, terminology structure and codes (Edition 4) – Annex А (Edition 3), G