Guidance on summary reports and issue-related analyses for medical devices: Overview

This guidance document was prepared to help medical device manufacturers understand and comply with sections 25, 39 and 61.4 to 61.6 of the Medical Devices Regulations. Two new requirements in the Regulations were added to ensure the continued monitoring of benefits and risks after a product is authorized for sale in Canada.

Publisher
Health Canada
Resources
2
Catalogue metadata updated
2024-03-30

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