Changes

*[[Media:Deck Information Session – Feb 2021 V2 EN.pdf|Information session: Regulations Amending the Medical Devices Regulations (February 2021)]]

*[[Media:Deck Information Session – Feb 2021 V2 EN.pdf|Information session: Regulations Amending the Medical Devices Regulations (February 2021)]]

*[[Media:Deck Post-market regulations – FRN – Jun 2021 V2 EN.pdf|Medical Devices Regulations: Foreign Risk Notification (June 2021)]]

*[[Media:Deck Post-market regulations – FRN – Jun 2021 V2 EN.pdf|Medical Devices Regulations: Foreign Risk Notification (June 2021)]]

*[[Media:MedTech_2021_Summary_Reports_GCwiki.pdf|Medical Devices Regulations: Summary Report (October 2021)]]

*[[Media:MedTech 2021 Summary Reports GCwiki.pdf|Medical Devices Regulations: Summary Report (October 2021)]]

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=== Summary Report ===

=== Summary Report ===

*[[Media:Questions_and_Answers_Summary_Report_GCwiki.pdf|Questions & answers – Summary Report]]

*[[Media:Questions and Answers Summary Report GCwiki.pdf|Questions & answers – Summary Report]]

== '''Forms''' ==

== '''Forms''' ==

=== Foreign risk notification (FRN) ===

=== Foreign risk notification (FRN) ===

*[[Media:HC medical device FRN Form V2 EN.pdf|Foreign Risk Notification (FRN) Form]]

*[https://www.canada.ca/content/dam/hc-sc/documents/services/drugs-health-products/reports-publications/medeffect-canada/foreign-risk-notification-medical-devices-form.pdf Foreign Risk Notification (FRN) Form]

*[[Media:FRM-0090 Authorization for medical devices mandatory problem foreign risk notification and recall reporting EN v22.docx|Permission for the importer to report on behalf of the manufacturer (Health Canada "FRM-0090")]]

*[[Media:FRM-0090 Authorization for medical devices mandatory problem foreign risk notification and recall reporting EN v22.docx|Permission for the importer to report on behalf of the manufacturer (Health Canada "FRM-0090")]]

[[fr:SCinstrmed]]

[[fr:SCinstrmed]]