Food and Drug Regulations (C.R.C., c. 870)
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Regulations are current to 2026-06-21 and last amended on 2026-06-17. Previous Versions
C.01.040.3 In deciding whether to amend the Prescription Drug List in respect of a drug, including by adding the drug to it or removing the drug from it, the Minister shall consider whether any of the following criteria apply with respect to the drug:
(a) supervision by a practitioner is necessary
(i) for the diagnosis, treatment, mitigation or prevention of a disease, disorder or abnormal physical state, or its symptoms, in respect of which the drug is recommended for use, or
(ii) to monitor a disease, disorder or abnormal physical state, or its symptoms, in respect of which the drug is recommended for use, or to monitor the use of the drug;
(b) the level of uncertainty respecting the drug, its use or its effects justifies supervision by a practitioner; or
(c) use of the drug can cause harm to human or animal health or a risk to public health and the harm or the risk can be mitigated by a practitioner’s supervision.
- SOR/2013-122, s. 10
- SOR/2017-18, s. 21(F)
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