Through A&C’s sustained focus on meeting the most stringent regulatory requirements, we are committed to meeting the needs of pharmaceutical and biopharmaceutical manufacturers.

A&C understands the unique processes of individual manufacturers and continues to provide custom solutions to support your specific manufacturing and quality objectives.

A&C prides itself on being known as a company that provides full transparency in the supply chain which is demonstrated through our EXCiPACT GMP & GDP certification. We also have been audited by Health Canada, hold a Drug Establishment License, and our manufacturing site is FDA registered. Our responsibility and role in safeguarding public health is the foundation of our quality management system which provides the confidence necessary in our supply of the highest quality excipients, process solutions, buffers and active pharmaceutical ingredients.

As part of A&C’s strategic focus, we have invested substantially in the development of our bioprocessing liquid and bulk handling capabilities. We remain committed to ensuring adherence to good manufacturing practices and full compliance in meeting the international regulatory requirements which are at the core of our business decisions.

We look forward to working with you and becoming your global GMP partner.

Our Team

A&C has been servicing the life sciences industry for more than five decades. Our team is highly experienced in pharmaceutical and biopharmaceutical custom ingredient development, ingredient manufacturing and buffer production.

Our Quality Assurance and Quality Control teams are formed by highly skilled and qualified experts with many years of  experience in the pharmaceutical industry. Their work ensures that our compliance with all pharmaceutical standards and requirements is constantly respected.