Optimizing Standards for Regulatory Use
A Proposed Document was released by the International Medical Device Regulators Forum (IMDRF) Standards Working Group.
This consultation closed on Thursday 24 May 2018.
Working Group Chair: Scott Colburn, USA
Thank you for your contribution aiming at the validation of the IMDRF document.
Consultation documents
- N51 - Optimizing Standards for Regulatory Use (PDF,756KB)
- N51 - Optimizing Standards for Regulatory Use (DOCX,986KB)
Please use the comments template to provide comments on the Proposed Document and email comments to Gail Rodriquez.