Medical Devices Regulations
Version of section 3 from 2026-10-01 to 2026-10-19:
3 (1) These Regulations also apply to an in vitro diagnostic product that is a drug or that contains a drug, as if the product were an in vitro diagnostic device.
(2) Subsection (1) does not apply to
(a) a drug listed in Schedule E or F to the Act;
(b) a drug listed in any of the schedules to the Controlled Substances Regulations; or
(c) a drug containing cannabis, as those terms are defined in subsection 1(2) of the Cannabis Regulations and subsection 2(1) of the Cannabis Act, respectively.
- SOR/2018-144, s. 371
- SOR/2025-246, s. 14
Page Details
- Date modified: