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Food and Drug Regulations

Version of section C.01.611 from 2006-03-22 to 2016-05-03:

  •  (1) The Director may, in writing, from time to time require the manufacturer of a drug recommended for administration to animals that may be consumed as food

    • (a) to file with him in respect of that drug a submission, in form and content satisfactory to the Director, describing in detail tests carried out to determine that no residues of the drug, except residues within the limits prescribed by these Regulations, remain in meat, meat by-products, eggs or milk; and

    • (b) to print on the principal display panel of the outer label, the inner label and the packaging insert, if any, that describes the drug, a warning that meat, meat by-products, eggs or milk from animals to which the drug has been administered cannot be sold for consumption as food unless there has elapsed since the administration of the drug a period of time specified by the Director, based on a review of the available data with respect to drug residue.

  • (2) No manufacturer shall sell a drug in respect of which the Director has required a warning to be printed pursuant to paragraph (1)(b) unless the manufacturer has complied with that request.

  • SOR/93-467, s. 2

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