Food and Drug Regulations
Version of section C.08.003.1 from 2006-03-22 to 2011-03-24:
C.08.003.1 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.08.002.1, 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
- Date modified: