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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.
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=== '''<big>Welcome!</big>''' ===
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This page was developed to share resources related to the Investigational Testing provisions under the Medical Devices Regulations.
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If you have questions, please contact Health Canada's Medical Devices Directorate at mdd.postmarket-postcommercialisation.dim@hc-sc.gc.ca.
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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.
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== Links to Online Resources ==
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