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DSA Consultants: Your Partner for Regulatory Affairs & GMP Quality Compliance.
If your company provides manufacturing, packaging, wholesale, distribution or importing services, your company is responsible to ensure compliance with the Canadian Food & Drugs Act.
DSA Consultants address every aspect of Drug, Medical Device, Natural Health Product and Cosmetic compliance.
At DSA Consultants, we know that in order to be successful, you can’t be everything to every arm of the healthcare industry. We only provide consulting services and aren’t distracted by other business activities. We specialize in specific industries in order to provide our clients with exceptional knowledge and service. We work in specific areas of the industry such as:
- Drug product submissions, labelling review, establishment licensing and GMP compliance.
- Medical device risk assessment & product registration submissions, labelling, establishment licensing, mandatory problem reporting and other areas of regulatory compliance.
- Natural health product assessment & labelling, product registration submissions, GMP compliance, and site licensing.
- Cosmetic labelling and product registrations
Our experts have extensive backgrounds in specific pharmaceutical and healthcare fields. Our Regulatory and Quality Consulting professionals bring their background and experience to the DSA team for the benefit of all our clients. We work with over 150 clients who rely on us to help them comply with Canadian Regulatory requirements.
Rely on DSA Consultants as your trusted partner for Canadian Regulatory Compliance.
We have over 20 years of experience in Canadian Regulatory Affairs and Quality Compliance. Put our industry experience to work for you today and find out why so many companies have chosen DSA as their trusted Regulatory Partner.
Contact DSA Consultants for more information about how we can assist you.


