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Food and Drug Regulations

Version of section C.10.004 from 2022-03-02 to 2023-01-25:

  •  (1) The following definitions apply in this section and in sections C.10.005 to C.10.011.

    designated drug

    designated drug means a drug that is set out in the List of Drugs for Exceptional Importation and Sale. (drogue désignée)

    drug

    drug means any of the following drugs for human use:

    • (a) drugs included in Schedule I, II, III, IV or V to the Controlled Drugs and Substances Act;

    • (b) prescription drugs;

    • (c) drugs that are listed in Schedule C or D to the Act; and

    • (d) drugs that are permitted to be sold without a prescription but that are to be administered only under the supervision of a practitioner. (drogue)

    foreign regulatory authority

    foreign regulatory authority has the same meaning as in subsection C.10.001(1). (autorité réglementaire étrangère)

    List of Drugs for Exceptional Importation and Sale

    List of Drugs for Exceptional Importation and Sale means the List of Drugs for Exceptional Importation and Sale that is published by the Government of Canada on its website, as amended from time to time. (Liste des drogues destinées aux importations et aux ventes exceptionnelles)

  • (2) In sections C.10.006 and C.10.009, batch certificate, fabricate, MRA country, package/label and recognized building have the same meanings as in subsection C.01A.001(1).

  • SOR/2021-199, s. 5
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