Natural Health Products Regulations

Version of section 51 from 2006-03-22 to 2018-04-03:

  •  (1) Every manufacturer, packager, labeller, importer and distributor shall

    • (a) have a quality assurance person who

      • (i) is responsible for assuring the quality of the natural health product before it is made available for sale, and

      • (ii) has the training, experience and technical knowledge relating to the activity conducted and the requirements of this Part; and

    • (b) investigate and record every complaint received in respect of the quality of the natural health product and, if necessary, take corrective action.

  • (2) Every natural health product shall be manufactured, packaged and labelled using only material that, prior to its use in the activity, has been approved for that use by a quality assurance person.

  • (3) Every natural health product shall be manufactured, packaged, labelled and stored using methods and procedures that, prior to their implementation, have been approved by a quality assurance person.

  • (4) Every lot or batch of a natural health product shall be approved by a quality assurance person before it is made available for sale.

  • (5) Every natural health product that is sold and subsequently returned to its manufacturer, packager, labeller, importer or distributor, as the case may be, shall be approved by a quality assurance person before that natural health product may be made available for resale.

Date modified: