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Category: Adverse Event Reporting – AER

New Zealand – Changes to Medical Device Adverse Event Reporting process

9 Oct, 2019 Marcelo Antunes Adverse Event, Adverse Event Reporting - AER, New Zealand, New Zealand Medicines and Medical Devices Safety Authority - MEDSAFE
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

22 Jul, 2019 Marcelo Antunes Adverse Event, Adverse Event Reporting - AER, International Medical Device Regulators Forum - IMDRF
IMDRF terminologies for categorized Adverse Event Reporting (AER): terms, terminology structure and codes (Edition 4) – Annex А (Edition 3), G
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