CDMO Services
Cell & Gene Therapy

Partner focused. Patient driven.

Your global provider of tailored CGT solutions.

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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.
  • Mar 24, 2025

    A Deep Dive into Flow Cytometry

    Precision-Driven Flow Cytometry: Advanced Technologies Ensuring Reliable Data for Complex Therapies. All flow cytometry assays performed in C3i are qualified and/or validated. Depending on the assays, three instruments are currently used: FACS Lyric, FACS Canto, or Accellix. During the qualification/validation, accuracy is verified using a known control (where reference values have already been established). Reproducibility […]

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  • Mar 10, 2025

    C3i announces the promotion of Julie Artigalas to Senior Manager – Client Accounts

    C3i is pleased to announce the promotion of Julie Artigalas to the position of Senior Manager – Client Accounts. This promotion marks a key milestone in our ongoing commitment to delivering strategic support and high-quality service to our partners, and reflects the significant impact Julie has had on the management of our clinical projects. Holding […]

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  • Feb 19, 2025

    C3i Center receives approval from the EMA to manufacture cell therapy products for the European market.

    C3i announces that it has obtained regulatory approval from the EMA (European Medicine Agency) to produce cell therapy treatments for the European market. The company received a certificate of Good Manufacturing Practice (GMP) compliance following an inspection of their Montreal facility by the European Medicines Agency. Therefore, C3i obtains a certificate of GMP (Good Manufacturing […]

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