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Food and Drug Regulations

Version of section G.02.074 from 2019-12-09 to 2026-09-30:


Marginal note:Explainable loss of controlled drug

 A licensed dealer that becomes aware of a loss of a controlled drug that can be explained on the basis of normally accepted business activities must record the following information:

  • (a) the name of the lost controlled drug and, if applicable, the brand name of the product or the name of the compound containing it;

  • (b) the form and quantity of the controlled drug and, if applicable, the form of the product or compound containing it, the strength per unit of the controlled drug in the product or compound, the number of units per package and the number of packages;

  • (c) the date on which the dealer became aware of the loss; and

  • (d) the explanation for the loss.

  • SOR/2019-171, s. 1

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