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Difference between revisions of "Investigational Testing Authorization"
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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]]. | 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]]. | ||
| − | == ''' | + | === '''<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)] | ||
| − | + | ||
| − | + | [[FR:Autorisation Dessai Experimental]] | |
Latest revision as of 11:09, 28 January 2026
Welcome!
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.
Forms
To access forms used by the Investigational Testing Authorization Division, click below:
