CPL Contract Pharmaceuticals Limited

Description

At CPL, scientific sophistication and experience come together with flexibility, responsiveness, and innovation. Our Product Development Services provide our customers with an end-to-end service offering - pharmaceutical development through commercial manufacturing and testing - with a wide range of support services, state-of-the-art analytical capabilities, and rigorous quality systems. Our team has extensive experience with challenging drug candidates with poor solubility, inherent instability, or low bioavailability.

CPL has been providing innovative leadership in the liquid and semi-solid market since 1991 with a reputation as one of the most service-oriented contract manufacturers in the pharmaceutical industry. CPL’s roots began in 1991, as a third party packaging contractor of pharmaceutical products, and quickly expanded into a 59,000 square-foot production plant in Mississauga, Ontario, Canada. By 1997, we had outgrown that building and acquired an 85,000 square-foot facility in Mississauga in partnership with Block Drug.

By joining our team at CPL, you are joining a company that improves the quality of life of the people that use our customer’s products. Every member of our organization is involved in meeting the needs of our customers and making sure the products are at highest levels of quality, while providing the highest levels of service.

Ken brings diverse experience and talent to his role in providing the leadership to position CPL in the forefront of the industry. Ken’s career with CPL began in 2000 as a member of the Board of Directors and in-house executive focusing primarily on corporate development and strategic planning. Prior to his tenure at CPL, Ken held executive positions for over 20 years in finance, manufacturing operations, marketing and general management in both large private and public companies.

Erika has been a part of the CPL team for over 15 years. She joined the company as our first GMP Specialist in Quality Assurance. Within Quality Assurance, Erika led Validation and Compliance prior to overseeing site compliance as Director of Quality Systems. She has been instrumental in the development of many of our GMP programs with particular emphasis on our often tested and highly respected cleaning, process and packaging validation programs. She also held the role of Manager, New Product Transfer. In January 2009, Erika became the Focus Factory Leader of the Green Factory.

Products & services

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