The technical document Terminologies for Categorized Adverse Event Reporting (AER): Terms, Terminology and Codes has been updated by The International Medical Device Regulators Forum (IMDRF) Adverse Event Terminology working group (AET WG).
The current update consists of 36 newly added terms, changes to 56 existing terms and the retirement of eight terms. Release notes that provide a high-level overview of specific code updates in the 2025 publication cycle are available from the IMDRF website.
IMDRF Updates Terminologies for Categorized Adverse Event Reporting
IMDRF Updates Terminologies for Categorized Adverse Event Reporting
The technical document that defines the categories for adverse event reporting for medical devices has been updated by the IMDRF.
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