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Food and Drug Regulations (C.R.C., c. 870)

Regulations are current to 2026-09-21 and last amended on 2026-06-17. Previous Versions

  •  (1) Every distributor referred to in paragraph C.01A.003(b) and importer of a drug in dosage form shall establish the period during which each drug in the package in which it is sold will comply with the specifications for that drug.

  • (2) Every fabricator and importer of an active ingredient shall establish the period during which each drug in the package in which it is sold will comply with the specifications for that drug.

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

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