Food and Drug Regulations
Version of section C.03.012 from 2018-04-04 to 2024-10-30:
C.03.012 On written request from the Minister, every fabricator, packager/labeller, tester, distributor referred to in paragraph C.01A.003(b) and importer of a drug shall submit protocols of tests together with samples of any lot or master lot of the drug before it is sold, and no person shall sell a lot of which the protocol or sample fails to meet the requirements of these Regulations.
- SOR/97-12, s. 27
- SOR/2018-69, s. 27
- Date modified: