Difference between revisions of "Investigational Testing Authorization"
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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 == | + | == '''Links to Online Resources''' == |
| + | Add link | ||
| + | |||
| + | == '''Questions & Answers''' == | ||
| + | Questions & answers documents were prepared in response to enquiries received. | ||
Revision as of 13:35, 17 July 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
Add link
Questions & Answers
Questions & answers documents were prepared in response to enquiries received.
