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Natural Health Products Regulations

Version of section 72 from 2006-03-22 to 2022-06-20:


 If the authorization to sell or import a natural health product for the purposes of the clinical trial is amended in accordance with subsection 71(5), the sponsor shall

  • (a) before commencing to sell or import the natural health product in accordance with the amended authorization

    • (i) cease to sell or import the natural health product in accordance with the existing authorization, and

    • (ii) maintain records concerning the information referred to in subparagraph 66(c)(ix), if any of that information has changed since it was submitted, and the information referred to in paragraph 66(f); and

  • (b) conduct the clinical trial in accordance with the amended authorization.


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