MEDSAFE – Medical Device Adverse Event Reporting
Posts published in “Adverse Event”
IMDRF terminologies for categorized Adverse Event Reporting (AER): terms, terminology structure and codes (Edition 4) – Annex А (Edition 3), G
October 22, 2020
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