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Food and Drug Regulations

Version of section C.04.015 from 2018-04-04 to 2020-06-17:


 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 of the drug before it is sold, and no person shall sell any lot of that drug if the protocol or sample fails to meet the requirements of these Regulations.

  • SOR/97-12, s. 37
  • SOR/2018-69, s. 27
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