At Cell-Easy, we provide end-to-end GMP manufacturing services for advanced therapy medicinal products (ATMPs), with a strong focus on compliance, scalability, and reliability.
We help biotech and pharma companies bring innovative cell therapies from the lab to the clinic by combining high-quality starting material sourcing, robust process development, and clinical-grade GMP production that meets international standards (MHRA, ANSM, EMA, FDA readiness).
Whether you need early clinical batches or large-scale production, our tailored solutions optimize your process, minimize risks, and accelerate time-to-clinic.


IMPD Approval for FIH Trial in Systemic Sclerosis – Cell Easy EU regulatory approval to administer Adipose-derived mesenchymal Stem Cells

Cell-Easy is pleased to welcome Mrs. Gisele Deblandre, formerly CSO at MaSTherCell, as Chief Scientific Officer Cell-Easy, a specialized contract

IUCT-Oncopole and Cell-Easy sign a MOU to accelerate cancer patient access to advanced cell-based therapy IUCT-Oncopole – Nouvelle fenêtre and Cell-Easy announced today the

Cell-Easy Appoints CDMO Expert Dr. Ribault to Its Board Cell-Easy is a leading contract development and manufacturing organization (CDMO) with

EMERCell & Cell-Easy sign a Strategic Agreement for the Scale-up and Manufacturing of NK-001 Emercell has selected Cell-Easy as a

Cell-Easy Launches OPTI-STEM for Cell Therapy Access The OPTI-STEM consortium led by CDMO Cell-Easy receives €7M from the French government