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IMDRF Principles and Practices for Medical Device Cybersecurity

A Proposed Document by the International Medical Device Regulators Forum (IMDRF) Medical Device Cybersecurity Working Group is provided below for public comment.

This consultation closes on Monday, 2 December 2019.

Working Group Chairs: Suzanne Schwartz, US FDA and Marc Lamoureux, Health Canada

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 send comments via email to Aftin: aftin.ross@fda.hhs.gov with the subject line 'IMDRF Consultation'.