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Food and Drug Regulations

Version of section C.01A.007 from 2021-09-16 to 2024-06-19:

  •  (1) The Minister may, on receipt of an application for an establishment licence, an amendment to an establishment licence or the review of an establishment licence, require the applicant to submit further details pertaining to the information contained in the application that are necessary to enable the Minister to make a decision.

  • (2) When considering an application, the Minister may require that

    • (a) an inspection be made during normal business hours of any building referred to in paragraph C.01A.005(1)(g) or (h); and

    • (b) the applicant, if a fabricator, a packager/labeller, a person who performs tests required under Division 2, a distributor referred to in paragraph C.01A.003(b) or an importer, supply samples of any material to be used in the fabrication, packaging/labelling or testing of a drug.

  • SOR/97-12, s. 5
  • SOR/2011-81, s. 4
  • SOR/2021-45, s. 5(F)

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