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Precursor Control Regulations

Version of section 91.92 from 2006-03-22 to 2025-12-16:

  •  (1) The person in charge of a hospital shall not permit a preparation or mixture containing a Class A precursor set out in column 1 of the schedule to be sold or provided to a patient or for the benefit of an animal under treatment as an in-patient or an out-patient of the hospital in a quantity, per transaction, that exceeds the maximum quantity, expressed as an absolute quantity or per package, specified for the contained precursor in column 2 of the schedule, unless the transaction is made under a prescription or another authorization of a practitioner practising in the hospital.

  • (2) The person in charge of the hospital shall keep the following information or ensure that it is kept:

    • (a) the name and quantity of the preparation or mixture provided when the prescription was filled;

    • (b) the name and address of the person for whom the prescription was issued;

    • (c) the date on which the prescription was filled; and

    • (d) the number assigned to the prescription.

  • SOR/2005-365, s. 58

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