Food and Drug Regulations
C.07.010 The manufacturer shall, with respect to a drug authorized to be sold under this Division,
(a) establish and maintain records, in a manner that enables an audit to be made, respecting the information described in section C.08.007; and
(b) provide to the Minister the reports referred to in section C.08.008.
- SOR/2005-141, s. 1
- Date modified: