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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Dec 08, 2025
Fit for Purpose: Ensuring Rigorous Validation in a GMP Environment
Read MoreIn the complex world of cell and gene therapy, the reliability of every analytical result depends on one essential principle: validation. Within C3i’s GMP framework, each assay, instrument, and dataset must demonstrate that it is fit for purpose, capable of delivering accurate, traceable, and reproducible results that withstand regulatory scrutiny, ensuring Rigorous Validation in a […]
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Dec 01, 2025
Precision at Speed: Molecular Assays for Safer Cell Therapies
Read MoreAs cell and gene therapy technologies advance, molecular assays have become essential for ensuring both speed and safety in product release. At C3i, these assays are designed with a single objective: to deliver rapid, validated data that regulators and clinicians can trust. The mycoplasma assay exemplifies this balance. Traditional compendial methods require a 28-day culture […]
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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, […]
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.