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Principles of Labeling for Medical Devices and IVD Medical Devices

A Proposed Document has been released by the International Medical Device Regulators Forum (IMDRF) Good Regulatory Review Practices Working Group.

This consultation will close on Wednesday 12 September 2018.

Working Group Chair: Melissa Torres, USA

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

Consultation documents

Please use the comments template to provide comments on the Proposed Document and email comments to Melissa Torres.