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Food and Drug Regulations

Version of section C.02.014 from 2013-11-08 to 2024-05-28:

  •  (1) Except in the case of a wholesaler or a distributor referred to in paragraph C.01A.003(a), no lot or batch of a drug shall be made available for further use in fabrication or for sale unless the person in charge of the quality control department approves the sale or the further use.

  • (2) A drug that is returned to its fabricator, packager/labeller, wholesaler, distributor referred to in section C.01A.003 or importer shall not be made available for further use in fabrication or for further sale unless the person in charge of the quality control department approves the further sale or further use.

  • (3) No lot or batch of a raw material or packaging/labelling material shall be used in the fabrication or packaging/labelling of a drug unless the person in charge of the quality control department approves the use.

  • (4) No lot or batch of a drug shall be reprocessed unless the person in charge of the quality control department approves the reprocessing.

  • SOR/82-524, s. 3
  • SOR/89-174, s. 8(F)
  • SOR/97-12, ss. 14, 55
  • SOR/2010-95, s. 5
  • SOR/2013-74, s. 9

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