Pharmascience | Quality Standards

Quality Standards

Committed to Quality

Our Quality & Compliance team is actively engaged in all stages of production from the inspection of raw materials, manufacturing, and packaging, straight through to distribution practices. Our team inspects, samples and analyzes raw materials and finished products to ensure compliance. It also scrutinizes factory operations to ensure that premises, systems, equipment, and processes all comply with Good Manufacturing Practices (GMP) requirements.

The Quality & Compliance team confirms that each batch of medication meets defined specifications before it can be released to customers.

Our 275+ dedicated employees within the Quality & Compliance team are proud to oversee every stage of production. This team of scientists, managers, specialists, analysts, and support staff understands the vital role it plays in delivering the highest levels of quality to all of our customers.

At Pharmascience, “Quality & Compliance” is not just part of our manufacturing process, it is the roadmap that guides our behaviours and helps us fulfill our commitments.

Samba Sow PharmD, MBA Vice President, Quality & Compliance

Highest Quality Standards Around the World

Pharmascience is committed to delivering the highest quality of products and service to our customers around the world. Our teams are up to date on the quality expectations of all of our international markets and our drugs, natural health products, and medical devices meet all market requirements where they are sold.


  • Drugs – Good Manufacturing Practices (GMP) described in Part C, Division 2, of the Food and Drug Regulations of Canada.
  • Natural Health Products – Natural Health Products Regulations of Canada.
  • Medical Devices – Canadian Medical Devices Regulations. Standard CAN / CSA-ISO 13485: 2016 entitled Medical devices – Quality management systems – Requirements for regulatory purposes.

United States

  • 21 CFR Part 210 – Current Good Manufacturing Practices in Manufacturing, Processing, Packing or Holding of Drugs.
  • 21 CFR Part 211 – Current Good Manufacturing Practices for Finished Pharmaceuticals.

European Community

Eudralex, Volume 4 – Good Manufacturing Practice (GMP) for Medicinal Products for Human and Veterinary use.


Manufactured to the highest Canadian standards, our locally produced products are available all across Canada.

Canadian Market


We consistently offer the same meticulous attention, care, and high-quality products to consumers in over 50 countries.

International Market