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Food and Drug Regulations

Version of section C.08.003.1 from 2011-03-25 to 2020-11-17:


 In examining a new drug submission, an extraordinary use new drug submission, an abbreviated new drug submission, an abbreviated extraordinary use new drug submission or a supplement to any of those submissions, the Minister may examine any information or material filed with the Minister by any person pursuant to Division 5 or section C.08.002, C.08.002.01, C.08.002.1, C.08.003, C.08.005 or C.08.005.1 to establish the safety and effectiveness of the new drug for which the submission or supplement has been filed.

  • SOR/95-411, s. 6
  • SOR/2001-203, s. 5
  • SOR/2011-88, s. 14
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