CDMO Services
Cell & Gene Therapy
Partner focused. Patient driven.
Your global provider of tailored CGT solutions.
C3i has built a one-stop shop in the development chain of Cell & Gene Therapy.
We work closely with our clients to manufacture products destined for patients all over the world. C3i prides itself on delivering, on time, quality results on behalf of its clients and for patients, advanced cell and gene products that meet regulatory requirements around the world.
Our Purpose
We work with our clients to ensure we put patients first. We are driven to perform our best knowing that the cells in our hands may be the patient's only chance at survival.
Our People
We are dedicated and highly trained personnel with over 15 years of experience in cell therapy and cGMP manufacturing.
Our Facility
C3i is the only fully validated cGMP center in Canada compliant with FDA, EMA, and Health Canada regulations with commercial capacity.
Fully integrated in-house and on-site services to ensure seamless communication between all parties
We are a CDMO that develops, translates, and manufactures complex cell and gene therapies with a very high success rate. Our strength lies in working with our partners to advance the industry’s ability to bring cell and gene therapy research to market.
We are an extension of your team
C3i works as part of your team proudly blurring the lines between “you“ and “us” to the most desirable “we.” We are the CDMO for cell and gene therapy that fills the gap between your research and innovative patient therapies.
Read the latest news
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Nov 25, 2025
Rapid and Reliable: Ensuring Quality Through Release Testing
Read MoreIn cell and gene therapy, every hour matters. The ability to test, qualify, and release a product quickly can directly impact a patient’s access to treatment. At C3i, release testing is designed to deliver fast, reliable results without compromising scientific or regulatory rigour. C3i’s Quality Control (QC) laboratory oversees every step of product testing, […]
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Nov 12, 2025
The C3i Center welcomes Bobby Boursiquot as its new Vice President of Commercialization
Read MoreThe C3i Center is proud to announce the appointment of Bobby Boursiquot, B.Sc., MBA, as Vice President of Commercialization. With over two decades of experience in scientific innovation and commercial growth, Mr. Boursiquot will lead the C3i Center’s initiatives to accelerate the transfer of cell and gene therapy discoveries to the marketplace. “Bobby’s rare combination […]
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Jun 04, 2025
Licensed to Deliver: DEL & EMA Explained
Read MoreWhat Do DEL and EMA Licenses Mean for Our Day-to-Day Operations? Our commercial manufacturing licenses allow us to manufacture and test cell therapy products for the commercial market. To achieve it, all our processes were reviewed and adjusted to meet the highest regulatory standards. The level of qualification/validation of manufacturing processes, equipment, facilities, analytical methods, […]
Make great strides in your career at C3i
C3i offers a wide range of opportunities for you to contribute to our mission of advancing cell and gene therapy.