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Four guidance documents are available to support the interpretation of the new or updated post-market provisions in the Medical Devices Regulations that were published in Canada Gazette Part II on December 23, 2020. | Four guidance documents are available to support the interpretation of the new or updated post-market provisions in the Medical Devices Regulations that were published in Canada Gazette Part II on December 23, 2020. | ||
| − | + | [[Media:Guidance document links Post-Market FINAL FR.pdf|Links to guidance documents]] | |
== Presentation slide decks == | == Presentation slide decks == | ||
Information sessions were offered by Health Canada in February 2021 related to the new post-market provisions. The presentation slide decks are available for viewing. | Information sessions were offered by Health Canada in February 2021 related to the new post-market provisions. The presentation slide decks are available for viewing. | ||
Revision as of 14:02, 1 June 2021
Welcome!
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, 2021.
If you have questions, please contact Health Canada's Medical Devices Directorate at hc.mdd.postmarket-postcommercialisation.dim.sc@canada.ca.
Links to guidance documents
Four guidance documents are available to support the interpretation of the new or updated post-market provisions in the Medical Devices Regulations that were published in Canada Gazette Part II on December 23, 2020.
Presentation slide decks
Information sessions were offered by Health Canada in February 2021 related to the new post-market provisions. The presentation slide decks are available for viewing.
Questions & answers
Questions & answers documents were prepared in response to enquiries received.
Foreign risk notification:
Forms
Forms have been created to support compliance with the new regulations.
