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Investigational Testing Authorization (view source)
Revision as of 10:25, 17 July 2023
, 10:25, 17 July 2023no edit summary
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.
=== '''<big>Welcome!</big>''' ===
This page was developed to share resources related to the Investigational Testing provisions under the Medical Devices Regulations.
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 Health Canada's Investigational Testing Authorization Division within the Medical Devices Directorate at it-ee@hc-sc.gc.ca.
== Links to Online Resources ==
