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Food and Drug Regulations

Version of section G.06.002.2 from 2018-04-04 to 2019-12-08:


 The manufacturer of a test kit that contains a controlled drug may apply for a registration number therefor by submitting to the Minister an application containing

  • (a) particulars of the design and construction of the test kit;

  • (b) a detailed description of the controlled drug and other substances, if any, contained in the test kit, including the qualitative and quantitative composition of each component;

  • (c) a statement of the proposed use of the test kit; and

  • (d) any further information and material that the Minister may require in order to satisfy himself that the test kit is one for which a registration number may be issued.

  • SOR/2018-69, s. 70

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