Government of Canada / Gouvernement du Canada
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Food and Drug Regulations

Version of section C.02.013 from 2013-11-08 to 2023-09-19:

  •  (1) Every fabricator, packager/labeller, wholesaler, distributor referred to in section C.01A.003 and importer of a drug shall have on their premises in Canada a quality control department that is supervised by personnel described in section C.02.006.

  • (2) Except in the case of a wholesaler or a distributor referred to in paragraph C.01A.003(a), the quality control department shall be a distinct organizational unit that functions and reports to management independently of any other functional unit, including the manufacturing, processing, packaging or sales unit.

  • SOR/82-524, s. 3
  • SOR/89-174, s. 8(F)
  • SOR/97-12, s. 55
  • SOR/2000-120, s. 10
  • SOR/2010-95, s. 4
  • SOR/2013-74, s. 9
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