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This page was developed to share resources related to the new post-market provisions under the '''''Medical Devices Regulations''''', published in Canada Gazette, Part II on December 23, 2020.
This page was developed to share resources related to the new post-market provisions under the '''''Medical Devices Regulations''''', published in Canada Gazette, Part II on December 23, 2020.
If you have questions, please contact Health Canada's Medical Devices Directorate at '''mdd.postmarket-postcommercialisation.dim@hc-sc.gc.ca'''.
If you have questions, please contact MDD's post-market division at '''mdd.postmarket-postcommercialisation.dim@hc-sc.gc.ca''' or the BSN Chairs at '''hpfb-bsn@hc-sc.gc.ca'''.
== '''Links to online resources''' ==
== '''Links to online resources''' ==
Information sessions have been offered by Health Canada related to the new post-market provisions. Presentation slide decks are available for viewing.
Information sessions have been offered by Health Canada related to the new post-market provisions. Presentation slide decks are available for viewing.
*[[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 Reports (October 2021)]]
*
*[[Media:Summary Reports - Tips and Tricks for Success (EN).pdf| Medical Devices Regulations: Summary Reports: Tips and Tricks for Success (June 2022)]]
== '''Questions & answers''' ==
== '''Questions & answers''' ==
=== Foreign risk notification (FRN) ===
=== Foreign risk notification (FRN) ===
*[[Media:Questions and Answers – FRN V2 EN.pdf|Questions & answers – Foreign Risk Notification (FRN)]]
*[[Media:Questions and Answers FRN EN 2023-09-07.pdf|Questions & answers – Foreign Risk Notification (FRN)]]
=== 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]]
== '''Updates''' ==
=== The language about summary reporting has changed in the Medical Devices Regulations. What is the difference? Have the requirements changed? ===
Health Canada amended sections 61.4 to 61.6 of the Medical Devices Regulations (summary reporting provisions) to clarify the language and to align with the summary reporting provisions introduced for Part 1.1 of the Medical Devices Regulations. The new regulations in Part 1.1 describe ongoing regulations that continue accelerated access to COVID-19 medical devices for which there is an urgent public health need without relying on temporary regulatory measures.
While the language in the summary reporting provisions has been revised to be clearer, the intent is the same. As such, the requirements have not changed.
To understand and comply with the regulatory requirements for summary reports, refer to our [https://www.canada.ca/en/health-canada/services/drugs-health-products/reports-publications/medeffect-canada/medical-device-reports-analyses-guidance/summary.html guidance document].
