• We are recognized leaders in Canadian Regulatory Consulting
• We help Manufacturers, Importers, Distributors and Wholesalers comply with the requirements of the Canadian Food and Drugs Act and Regulations
• Our Team of Consultants have held prior positions with Health Canada and Industry
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DSA Consultants is A Key Piece of Your Business Puzzle for meeting the Regulatory Process in the Drug Industry.

What is a Drug?

The registration and sale of drug products in Canada is regulated by Part C of the Food and Drug Regulations. The Canadian Food and Drugs Act defines a drug as follows:

“drug” includes any substance or mixture of substances manufactured, sold or represented for use in

• (a) the diagnosis, treatment, mitigation or prevention of a disease, disorder or abnormal physical state, or its symptoms, in human beings or animals,
• (b) restoring, correcting or modifying organic functions in human beings or animals, or
• (c) disinfection in premises in which food is manufactured, prepared or kept;

With respect to drugs, we offer a wide range of services for;

Product Submissions Click here, for more details.	Labelling Review Click here, for more details.	Establishment Licensing Click here, for more details.	Quality Assurance⁄Quality Control Click here, for more details.

Contact us today to find out how we can help you navigate the Canadian Regulatory Framework with respect to drug products. For more information on services offered, click here to request a copy of our free brochure.