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Posts published in “Adverse Event”

New Zealand – Changes to Medical Device Adverse Event Reporting process

By Marcelo Antunes on October 9, 2019

MEDSAFE – Medical Device Adverse Event Reporting

IMDRF proposed document – IMDRF terminologies for categorized Adverse Event Reporting (AER): terms, terminology structure and codes (Edition 4) – Annex А (Edition 3), G

By Marcelo Antunes on July 22, 2019

IMDRF terminologies for categorized Adverse Event Reporting (AER): terms, terminology structure and codes (Edition 4) – Annex А (Edition 3), G