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Food and Drug Regulations

Version of section G.04.002 from 2019-12-09 to 2023-01-25:


Marginal note:Record of controlled drugs sold or provided

  •  (1) A practitioner who sells or provides a controlled drug to a person for self-administration or for administration to an animal shall, whether or not the practitioner charges for the drug, keep a record showing the name and quantity of the controlled drug sold or provided, the name and address of the person to whom it was sold or provided and the date on which it was sold or provided if the quantity of the controlled drug exceeds

    • (a) three times the maximum daily dosage recommended by the manufacturer or assembler of the controlled drug; or

    • (b) three times the generally recognized maximum daily therapeutic dosage for that controlled drug if the manufacturer or assembler has not recommended a maximum daily dosage.

  • Marginal note:Accessibility of record

    (2) A practitioner who is required by this section to keep a record shall keep the record in a place, form and manner that will permit an inspector readily to examine and obtain information from it.

  • SOR/88-482, s. 4(F)
  • SOR/2004-238, s. 24
  • SOR/2019-171, s. 14
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