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Food and Drug Regulations

Version of section C.02.028 from 2013-11-08 to 2024-03-06:

  •  (1) Every distributor referred to in paragraph C.01A.003(b) and importer of a drug in dosage form shall monitor, by means of a continuing program, the stability of the drug in the package in which it is sold.

  • (2) Every fabricator and importer of an active ingredient shall monitor, by means of a continuing program, the stability of the drug in the package in which it is sold.

  • SOR/82-524, s. 3
  • SOR/97-12, s. 58
  • SOR/2013-74, s. 14

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