Guidance Document: Pre-market Requirements for Medical Device Cybersecurity - Summary
Information
Type
Guidance
Regulated products
Medical Devices
Topics
Medical Devices Guidance Documents, Health And Safety
Published
March 10, 2021
Last updated
March 19, 2021
Description
Guidance document is intended to provide advice to manufacturers and regulatory representatives on the practices, responses and mitigation measures, which can improve the cybersecurity of their medical device.
Tags
Organization
Country / Region
Canada
License
Open Government License 2.0 (Canada)