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RPS - Common Data Elements for Medical Device Identification

A proposed document has been released by the International Medical Device Regulators Forum (IMDRF) Regulated Product Submission (RPS) Working Group.

This consultation has now closed.

Working Group Chair: Ms Nancy Shadeed

Consultations

Please submit comments on the proposed document to the Working Group Chair, Ms Nancy Shadeed, using the comments template:

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