Medical Devices Regulations
Version of section 68.23 from 2024-01-03 to 2024-05-01:
68.23 The Minister may request that the manufacturer of a medical device who has submitted an application for an authorization or the holder of an authorization submit to the Minister, within a specified time limit, any additional information or documents or any material, including samples, that is necessary to enable the Minister to determine whether to issue, amend or cancel the authorization.
- SOR/2023-19, s. 7
- SOR/2023-277, s. 25
- Date modified: