Natural Health Products Regulations
28 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 establishing that they comply with the requirements set out in Part 3.
- SOR/2021-46, s. 17(F)
- SOR/2021-46, s. 19(E)
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