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Food and Drug Regulations

Version of section C.02.018 from 2006-03-22 to 2013-11-07:

  •  (1) Each lot or batch of a drug shall, prior to its availability for sale, be tested against the specifications for that drug.

  • (2) No lot or batch of a drug shall be available for sale unless it complies with the specifications for that drug.

  • (3) The specifications referred to in subsections (1) and (2) shall

    • (a) be in writing;

    • (b) be approved by the person in charge of the quality control department; and

    • (c) comply with the Act and these Regulations.

  • SOR/82-524, s. 3

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