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Site Licensing

All companies in Canada who want to manufacture, package, label or import a natural health product for sale must have a site licence (SL) that has been issued by Health Canada. Foreign sites performing these activities must be listed as approved foreign sites on a Canadian Company's SL.

In order to apply for a SL, you must provide detailed information to the Natural Health Products Directorate (NHPD) which shows that both your site and any foreign sites are compliant with NHP GMPs.

There are many options for establishing evidence of GMP compliance, including but not limited to the Quality Assurance Report or QAR. DSA can either prepare your QAR or review and update a QAR that has been prepared by your staff.

NHPD reviews your QAR or other evidence of GMP compliance, and if acceptable, will use this as the basis for issuing your Site Licence.

Assessment & Labelling Product Registrations GMP Compliance Site Licensing

Assessment & Labelling

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Product Submissions

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GMP Compliance

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Complaints and Adverse Reactions

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Contact us today to find out how we can help you apply for a Site Licence or help you obtain evidence of GMP Compliance. For more information on services offered, click here to request a copy of our free brochure.

Count on DSA Consultants to save you time and money…
and cut through the red tape of government regulations.

Call DSA Consultants today to discuss your unique professional needs.

(905) 827 - 0057
5006 South Service Road, Unit #6
Burlington, ON, L7L 5Y7

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