Xcell Therapeutics - Creators of CellCor™, a serum-free chemically defined media composed of over 200 known compounds. - Distributed in the UK & Ireland by Caltag Medsystems
Xcell Therapeutics Inc.
Xcell Therapeutics is a leading provider of advanced cell culture solutions, dedicated to supporting the biotechnology industry's research, development, and expansion of cells.
Recognising the critical importance of a well-optimised culture environment, Xcell Therapeutics has developed CellCor™, a series of Serum-Free Chemically Defined Media and Chemically Defined Animal-Origin-Free Medium.
Manufactured under stringent GMP-compliant conditions, CellCor™ ensures consistency and reliability, helping researchers achieve their cell culture objectives more effectively.
From early-stage research to clinical applications and therapeutic development, Xcell Therapeutics remains committed to delivering high-quality products that enhance the success of your cell culture processes.
CellCor™ Media
Xcell Therapeutics offer a variety of media for cell and gene therapies and exosome therapy.
The CellCor™ MSC CD AOF is an MSC-specific culture medium that is completely animal origin free. This launch enabled them to offer top-tier products that align with recent regulatory changes in the rapidly evolving field of cell therapy.
See all CellCor™ Media Available
| Product | CellCor™ MSC CD AOF | CellCor™ EXO CD | CellCor™ Kera CD AOF | CellCor™ DPC CD |
|---|---|---|---|---|
| Cat.No | YSP018(RUO) YSP023(GMP) | YSP017 | YSP019 | YSP007 |
| Volume | 500 mL | 500 mL | 500 mL | 500 mL |
| Grade | RUO, GMP | RUO | RUO | RUO |
| Phenol-red | O | O | O | O |
| Storage | – 20°C | 2 – 8°C | – 20°C | – 20°C |
| Shelf Life | 12 months | 12 months | 12 months | 12 months |
| Cell type | Human MSC Animal MSC | Human MSC derived exosome | Human Keratinocyte | Human Dermal Papilla Cell |
| Supplement | X | X | X | X |
| Coating | X | X | X | X |
Quality assurance from Xcell Therapeutics
Xcell Therapeutics quality control (QC) system adheres to globally recognised standards, ensuring compliance with international regulatory guidelines throughout the product development pipeline.
| RUO grade | GMP grade | |
|---|---|---|
| Application | Research & development, Preclinical research | IND, Commercialization |
| Quality system | ISO9001/ISO13485 Certified | ISO9001/ISO13485 Certified |
| Production | ISO certified facilities | ISO certified facilities |
| Research-grade materials or reagent grade | Vendor audit & Confirmation of supplier certification acquisition | |
| – | In operation Environment monitoring | |
| Quality control | Chemical testing | Chemical testing |
| Sterility testing | Sterility testing | |
| Mycoplasma testing | Mycoplasma testing | |
| Endotoxin testing | Endotoxin testing | |
| Performance testing | Performance testing | |
| 10th Production Identification testing | Identification testing (with acceptance criteria), CoA | |
| – | Other physical and chemical tests | |
| Validation | Validated key equipment | Validated key equipment |
| Validated key analytical instrument | Validated key analytical instrument | |
| – | Validated key Manufacturing process | |
| – | Validated key analytical methods | |
| Stability | First production 1 batch Long-Term Stability | Process Validation 3 Batch Long-Term Stability |
| – | In-use vertical stability test | |
| Documentation | Certificate of Analysis (CoA) | Certificate of Analysis (CoA) with ISO certification mark |
| Safety Data Sheets (SDS) | Safety Data Sheets (SDS) | |
| – | Certificate of Origin (CoO) | |
| – | Regulatory Support Files (RSF) | |
| – | Drug Master File (DMF) |