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Natural Health Products Regulations

Version of section 28 from 2006-03-22 to 2021-03-30:


 An application for a site licence shall be submitted to the Minister and shall contain the following information and documents:

  • (a) the name, address and telephone number, and if applicable, the facsimile number and electronic mail address of the applicant;

  • (b) a statement specifying which one or more of the activities of manufacturing, packaging, labelling or importing the applicant is proposing to conduct;

  • (c) if the applicant is proposing to manufacture, package or label a natural health product, the address of each building in which each activity is proposed to be conducted;

  • (d) if the applicant is proposing to import a natural health product, the address of each building in which that natural health product is proposed to be stored;

  • (e) for each activity specified under paragraph (b), a statement indicating whether or not the applicant is proposing to conduct the activity in respect of a natural health product in sterile dosage form; and

  • (f) in respect of the buildings, equipment, practices and procedures used to conduct each activity specified under paragraph (b), a report from a quality assurance person demonstrating that they comply with the requirements set out in Part 3.


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