The CDMO Expert in Cell Therapy Products
Cell-based therapies are not conventional Biologics, they are living drugs...requiring cutting-edge expertise in Cell Biology
By combining solid technological and scientific knowledge of cell culture with conventional, regulatory-supervised CDMO services, Cell-Easy's teams support you to translate your laboratory proof-of-concept into a succesful first-in-human clinical trial.
A proven track record in various cell types
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Clinical grade cGMP Batches
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Cell types:T-Cells, NK-Cells, iPS Cells, MSCs, Macrophages, immortalized cell lines
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Process & Anaytical method Development Programs
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successfulTech Transfer
How SCIENCE plays out at Cell-Easy ?
- 300+ cumulated years of cell culture experience
- Teams = PhDs, Engineers, Technicians in Cell Biology
- 70+ Technologies for Process & Analytics Development
- 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
What's new at Cell-Easy
News
May 14, 2024
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Contact
Tel : +33 534 276 550
Address : Cell-Easy SAS, 4 bis avenue Hubert Curien, 31100 Toulouse, France
Mail : info@cell-easy.com