The CDMO Expert
in Cell Therapy
Products
Cell-based therapies are not conventional Biologics,
they are living drugs
…requiring cutting-edge expertise in Cell Culture.
Clinical Doses
manufactured in our state-of-the-art GMP facilities
Cell types
T cells, NK cells, T regs, MSCs, iPS cells, Macrophages, immortalized cell lines,…
Development Programs
Process Development, Optimization, Scale up.
Analytical & Potency test development.
ATMP Developers
TRUST US
from academic, to Biotech and Pharma companies
Our CDMO/CRO Services
How SCIENCE plays out at Cell-Easy ?
By combining solid technological and scientific knowledge in CELL CULTURE with conventional regulatory-controlled CDMO services, Cell-Easy’s multi-disciplinary team support you in transforming your laboratory proof-of-concept into a successful first-in-human clinical trial.
- Teams = PhDs, Engineers, Technicians in Cell Biology
- 70+ Technologies for Process & Analytics Development
- REGULATORY support adapted to cell products
- CMC driven by cell variability
- From concept to First-in-Human and beyond
- A dedicated Project Manager
- Co-define a robust roadmap
- Share Risks & Gaps during weekly meeting
- Avoid Change of Scope
- Accelerate Process Development/Scale-up with our Platforms
- Access expertise on 50+ different technologies
- Pre-established contract with providers
- Beyond agreements (NDA, MSA, QTA) our internal confidential policy protect your industrial secret
- As a fee for service CDMO, no IP is shared
- All documentation/production is Yours
- Respect TIMELINES
- Meet BUDGET
- Bring continous CMC and REGULATORY support
- Your SUCCESS is our goal
Contact
Tel : +33 534 276 550
Address : Cell-Easy SAS, 4 bis avenue Hubert Curien, 31100 Toulouse, France
Mail : info@cell-easy.com