Government of Canada / Gouvernement du Canada
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Food and Drug Regulations

Version of section C.02.013 from 2010-04-29 to 2013-11-07:

  •  (1) Every fabricator, packager/labeller, wholesaler, distributor referred to in paragraph C.01A.003(b) 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, 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

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