De-Risk & Accelerate Your Journey To The Clinic With Your Cell Therapy CDMO Partner
We support academic laboratories, biotechs and pharma companies through development and GMP challenges, helping to reduce risk, speed up timelines, and build strong, trusted collaborations so you can focus on what matters: advancing your therapy with clarity and peace of mind.
1000+
Clinical doses
manufactured in our GMP facility
15
Cell Types handled
T cells, NK cells, T regs, MSCs, iPS, immortalized cell lines…
50+
Development Programs
Process Development, Optimization, Scale up, Analytical & Potency test development
Cell-Based Therapies Are Not Conventional Drugs. They’re Living Treatments
ATMP development is challenging, and every decision from process design to CMC strategy, can affect patient safety, regulatory approval, and trials success. That’s why our clients rely on us at every stage: to navigate complexity, reduce risk, and move their therapies forward with confidence.
Cell types handled: We handle both autologous and allogeneic, engineered (CAR/TCR) and non engineered (-T / -NK ; MSC/iPSc)
Technology agnostic: We operate independently of any specific platform or system, allowing us to adapt to your existing technologies and processes
Regulatory compliance: We ensure regulatory compliance at every stage, following ICH Q2 (R1), European Pharmacopeia, EMA/MHRA, and US Pharmacopeia standards, with a proven track record of successful audits.
CDMO Services To Accelerate Your Cell Therapy Development
Process Diagnostic
& Development
Analytical Development
cGMP Cell Banking
cGMP Manufacturing
Case Study: Solving the Scale-Up Barrier: How We Engineered a High-Yield, In Vivo-Ready T-Cell Process
Scaling up a T-cell therapy from lab-scale to large-scale manufacturing is challenging. Traditional T-flask methods consume excessive resources, require extensive manual work, and increase contamination risks. Our goal was to transform a small-scale proof-of-concept into a robust, scalable process suitable for in vivo studies.
Latest news
Stay on top of our latest breakthroughs.
CHU Toulouse and Cell-Easy Receive Regulatory Approval of A3D: A Phase 1 Trial Using CellReady® in Alzheimer’s Disease
Learn more: CHU Toulouse and Cell-Easy Receive Regulatory Approval of A3D: A Phase 1 Trial Using CellReady® in Alzheimer’s DiseaseCHU Toulouse and Cell-Easy Receive Regulatory Approval of A3D: A Phase 1 Trial Using CellReady® in Alzheimer’s Disease Cell-Easy, a
Cell-Easy Expands its GMP Cell Therapy Manufacturing Facility to Support Growing Client Demand
Learn more: Cell-Easy Expands its GMP Cell Therapy Manufacturing Facility to Support Growing Client DemandCell-Easy Expands its GMP Cell Therapy Manufacturing Facility to Support Growing Client Demand New state-of-the-art class-B cleanrooms, development labs, and
CTA Approval to initiate ALLOFIST
Learn more: CTA Approval to initiate ALLOFISTCTA Approval to initiate ALLOFIST CHU Toulouse receives CTA Approval to initiate ALLOFIST, a Phase 1/2 Trial based on Cell-Easy’s
They trusted us
Let’s talk about your project
Let’s turn your vision into a reality.
Phone: +33 534 276 550
Address: Cell-Easy SAS, 4 bis avenue Hubert Curien,
31100 Toulouse, France
Mail: info@cell-easy.com
