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Food and Drug Regulations

Version of section C.07.010 from 2006-03-22 to 2014-05-15:


 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
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