Difference between revisions of "Investigational Testing Authorization"
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* [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)] | * [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]] | * [[Media:Investigational_Testing_Notification_Form.docx|Investigational Testing Notification Form]] | ||
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Revision as of 14:22, 30 August 2023
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.
Links to Online Resources
For more information regarding Investigational Testing Authorizations please review the following resources:
Forms
To access forms used by the Investigational Testing Authorization Division, click below:
