De-Risk & Accelerate Your Journey To The Clinic With Your Cell Therapy CDMO Partner

manufactured in our GMP facility

T cells, NK cells, T regs, MSCs, iPS, immortalized cell lines…

Process Development, Optimization, Scale up, Analytical & Potency test development

Four technicians working in a GMP manufacturing environment. One is performing manipulations inside a biosafety cabinet performing manipulations, while the other three stand in the background.- Cell-Easy

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.

  • betacure_Cell-Easy

    Cell-Easy Launches an iPSC-Derived Beta Cell Program to Tackle Scale-Up Challenges

    Cell-Easy Launches an iPSC-Derived Beta Cell Program to Tackle Scale-Up Challenges Backed by a €12M Bpifrance grant, the program builds a GMP-compatible manufacturing platform for iPSC-derived cell therapies directly applicable to biotech and pharma iPSC programs. Toulouse, 2026 April 14th Tackling one of the main bottlenecks in iPSC-derived therapies Scale-up remains one of the most…

    Learn more: Cell-Easy Launches an iPSC-Derived Beta Cell Program to Tackle Scale-Up Challenges
  • CHU Toulouse Cell Easy

    CHU Toulouse and Cell-Easy Launch A-MUSE, a Phase 1/2 Clinical Trial Evaluating the CellReady® Allogeneic MSC Platform in Systemic Sclerosis

    CHU Toulouse and Cell-Easy Launch A-MUSE, a Phase 1/2 Clinical Trial Evaluating the CellReady® Allogeneic MSC Platform in Systemic Sclerosis Toulouse, January 22, 2026 — Cell-Easy, a CDMO specialized in the development and GMP manufacturing of Advanced Therapy Medicinal Products (ATMPs), announces a new clinical milestone achieved in close collaboration with Toulouse University Hospital (CHU Toulouse).…

    Learn more: CHU Toulouse and Cell-Easy Launch A-MUSE, a Phase 1/2 Clinical Trial Evaluating the CellReady® Allogeneic MSC Platform in Systemic Sclerosis
  • CellReady

    CHU Toulouse and Cell-Easy Receive Regulatory Approval of A3D: A Phase 1 Trial Using CellReady® in Alzheimer’s Disease

    CHU Toulouse and Cell-Easy Receive Regulatory Approval of A3D: A Phase 1 Trial Using CellReady® in Alzheimer’s Disease Cell-Easy, a Contract Development and Manufacturing Organization (CDMO) specialized in advanced cell therapies, announces that its allogeneic adipose-derived mesenchymal stem cell product, CellReady®, will be investigated in a newly approved Phase 1 clinical trial for Alzheimer’s disease.…

    Learn more: CHU Toulouse and Cell-Easy Receive Regulatory Approval of A3D: A Phase 1 Trial Using CellReady® in Alzheimer’s Disease