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Investigational Testing Authorization (view source)
Revision as of 11:23, 31 August 2023
, 11:23, 31 August 2023no edit summary
This page was developed to share resources related to the Investigational Testing provisions under the Medical Devices Regulations.
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 Investigational Testing Authorization Division within the Medical Devices Directorate at it-ee@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 ==
=== '''<big>Links to Online Resources</big>''' ===
For more information regarding Investigational Testing Authorizations please review the following resources:
* [https://www.canada.ca/en/health-canada/services/drugs-health-products/medical-devices/application-information/guidance-documents/investigational-testing-authorizations-guidance.html Applications for Medical Device Investigational Testing Authorizations Guidance Document]
=== '''<big>Forms</big>''' ===
To access forms used by the Investigational Testing Authorization Division, click below:
* [https://www.canada.ca/content/dam/hc-sc/documents/services/drugs-health-products/medical-devices/application-information/forms/new-ita-form_fillablePDF_EN-Nov07.pdf Application for New Investigational Testing Authorization (ITA)]
* [[Media:Investigational_Testing_Notification_Form.docx|Investigational Testing Notification Form]]
[[FR:Autorisation Dessai Experimental]]
