Quality and Compliance

A Commitment to Quality, A Record of Success

When you choose Atlas Pharmaceutical as your contract pharmaceutical development and manufacturing partner, your work will be held to the highest quality standards. Our quality team works closely with you to monitor all key activities, anticipate your needs and investigate challenges and opportunities to provide solutions that ensure your success.

Our quality team provides GMP oversight by administering quality systems and best practices concerning elements such as corrective action and preventive action (CAPA), complaints, applied pharma research (APR), training deviations, stability testing and internal audit programs.



Atlas Pharmaceutical’s outstanding regulatory compliance record serves as the foundation of our organization. Our management team has years of experience in pharmaceutical manufacturing for international markets and regulatory affairs. We provide oversight of regulatory compliance by administering a meticulous internal audit program, and we provide support for regulatory and client inspections and vendor auditing activities. A comprehensive set of standard operating procedures guides all key activities and keeps us compliant with the Health Canada Establishment License, precursor license and site license for dietary supplement.

Our focus on continuous training and investment in quality systems ensures that products developed and manufactured at Atlas live up to the most rigorous quality standards.


Regulatory Accreditations

  • Health Canada Establishment License





Atlas ImpEx/ Atlas R & D Inc.

35 Lingard Road, Unit # 2

Cambridge, Ontario N1T 2H4 Canada

Toll Free: 1 855 620-3782

Phone: +1 (519) 740-8508

Phone: +1  (226)  319-0400

Fax: +1 (519) 224-3425