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Food and Drugs Act

Version of section 21.8 from 2023-06-22 to 2024-10-30:


Marginal note:Health care institutions to provide information

  •  (1) A prescribed health care institution shall provide the Minister, within the prescribed time and in the prescribed manner, with prescribed information that is in its control about a serious adverse drug reaction that involves a therapeutic product or a medical device incident that involves a therapeutic product.

  • Marginal note:Definition of therapeutic product

    (2) Despite the definition therapeutic product in section 2, in subsection (1) therapeutic product means a drug or device or any combination of drugs and devices, but does not include a natural health product within the meaning of the Natural Health Products Regulations.

  • 2014, c. 24, s. 5
  • 2023, c. 26, s. 502

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