CPL is a leading contract development and manufacturing organization (CDMO) that provides development, manufacturing, packaging, and testing of non-sterile liquid and semi-solid pharmaceutical and regulated OTC products.  We have two facilities located in Mississauga, Ontario, Canada including our manufacturing & development site and our QC/office site. Our site segregation and controls allow for the handling and processing of many specialized materials including flammable materials, light or oxygen sensitivity, and hormones.  Our facilities are registered with the FDA and Health Canada and are routinely audited by regulatory agencies as well as our customers.  By offering a full-spectrum partnership – from development to commercial production – CPL creates strategic relationships with our customers that creates mutual benefits.

Manufacturing

Pharmaceutical

Contract Pharmaceuticals Limited

Jan Sahai

David Tyler

Brian Lankadurai

John Huang

Abu Thomas

Shannon Meijer

Manny Cordeiro

John Wilkening

The Development and Engineering Team at Contract Pharmaceuticals Limited (CPL) focuses on the end-to-end development and optimization of non-sterile liquid and semi-solid pharmaceutical products. This includes conducting analytical and skin lab research, ensuring process validation, and leading product development initiatives. They collaborate to create efficient, regulatory-compliant manufacturing processes that meet both FDA and Health Canada standards, thereby supporting CPL’s mission of providing high-quality pharmaceutical solutions to their clients.

Development and Engineering Team

Quality Assurance and Quality Control

Scientists and Researchers

Leadership Team

Development and Engineering Team

About

Team members

Other teams at Contract Pharmaceuticals Limited

Quality Assurance and Quality Control

Scientists and Researchers

Leadership Team