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IMDRF Terminologies for Categorized Adverse Event Reporting: terms, terminology and codes

A Proposed Document has been released by the International Medical Device Regulators Forum (IMDRF) Adverse Events Working Group.

This consultation will close on Friday 2 December 2016.

Working Group Chair: Hiroshi Ishikawa, Japan

Thank you for your contribution aiming at the validation of the IMDRF document.

Consultations

Please use the comments template to provide comments on the Proposed Document and email comments to imdrf-aewg-chair@pmda.go.jp.