Foreign risk notification for medical devices guidance document: Background

Information

Type

Miscellaneous

Regulated products

Medical Devices

Published

June 1, 2021

Last updated

June 10, 2022

Description

This guidance document is to help manufacturers and importers of medical devices understand and comply with the regulatory requirements on foreign risk notification (FRN).

Organization

Country / Region

Canada

License

Open Government License 2.0 (Canada)

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