Difference between revisions of "Investigational Testing Authorization"
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To access forms used by the Investigational Testing Authorization Division, click below: | 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)] | * [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: | + | * [[Media:==PUT THE FILE NAME HERE==|Investigational Testing Notification Form]] |
Revision as of 15:17, 28 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:
