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Food and Drug Regulations

Version of section C.03.012 from 2006-03-22 to 2018-04-03:


 On written request from the Director, 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
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