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Food and Drug Regulations

Version of section C.02.015 from 2006-03-22 to 2010-04-28:

  •  (1) All fabrication, packaging/labelling, testing, storage and transportation methods and procedures that may affect the quality of a drug shall be examined and approved by the person in charge of the quality control department before their implementation.

  • (2) The person in charge of the control department shall cause to be investigated every complaint on quality that is received and cause corrective action to be taken where necessary.

  • (3) The person in charge of the quality control department shall cause all tests or examinations required pursuant to this Division to be performed by a competent laboratory.

  • SOR/82-524, s. 3
  • SOR/97-12, s. 15
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