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'''Welcome!'''
'''<big>Welcome!</big>'''
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.
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.
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.
=== Foreign risk notification: ===