Food and Drug Regulations

Version of section C.02.006 from 2006-03-22 to 2018-04-03:


 Every lot or batch of a drug shall be fabricated, packaged/labelled, tested and stored under the supervision of personnel who, having regard to the duties and responsibilities involved, have had such technical, academic and other training as the Director considers satisfactory in the interests of the health of the consumer or purchaser.

  • SOR/82-524, s. 3;
  • SOR/85-754, s. 2;
  • SOR/97-12, s. 52.
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