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Food and Drugs Act

Version of section 21.71 from 2020-05-23 to 2022-09-11:


Marginal note:Duty to publicize clinical trial information

 The holder of a therapeutic product authorization referred to in paragraph 30(1.2)(c) shall ensure that prescribed information concerning the clinical trial is made public within the prescribed time and in the prescribed manner.

  • 2014, c. 24, s. 3
  • 2019, c. 29, s. 168
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