CDMO Services
Cell & Gene Therapy

Partner focused. Patient driven.

Your global provider of tailored CGT solutions.

Let’s talk
About Us

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.

News

Read the latest news

Learn more about how C3i takes part in the development of new cell and gene therapies.
  • Apr 10, 2026

    C3i at the 4th CellCAN Strategic Forum 2026 in Laval

    From April 7 to 9, 2026, C3i took part in the 4th Pan-Canadian Strategic Forum on Cell and Gene Therapies, organized by CellCAN at the Sheraton Laval & Convention Center.   The event brought together key players in the sector, including scientists, innovators, and partners from the cell and gene therapy biomanufacturing ecosystem, around a […]

    Read More
  • Mar 31, 2026

    C3i Attended the 2026 Summit4CI

    From March 29 to 31, 2026, C3i participated in the Summit for Cancer Immunotherapy (Summit4CI), organized by BioCanRx in Vancouver. This annual event brings together scientists, clinicians, industry leaders, and patient advocates committed to advancing immuno-oncology.   At the event, Jamie Sharp, Director of Business Development at C3i, represented the organization to engage with the […]

    Read More
  • Mar 11, 2026

    Preparing for Regulatory Inspection in Cell and Gene Therapy Manufacturing

    Regulatory inspections represent a critical validation of manufacturing quality systems in cell and gene therapy. These inspections assess not only whether procedures exist, but whether they are effectively implemented and consistently followed. For advanced therapy manufacturers, inspection readiness reflects the strength, maturity, and reliability of the entire Quality Assurance framework. At C3i, inspection readiness begins […]

    Read More