IMDRF Releases Consolidated Adverse Event Reporting Terms

The International Medical Device Regulators Forum (IMDRF) has released a consolidated document for Categorized Adverse Event Reporting (AER), now available in a single file for easier reference. Previously, each annex was published separately, but this update brings all annexes together, with each annex retained on a separate sheet within the main document. The structure and layout of the annexes remain unchanged from the previous release.

You can download the consolidated Annexes A-G here.