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Experience rapid transition from your discovery to GMP compliant production
Our Team includes specialist scientists with 10+ years of experience in culturing primary mammalian cells, and QA experts to help transfer your discoveries into a regulatory-compliant GLP and GMP technology.
Our GMP facilities are based in Central Europe with a track record of delivering finished products to International Markets.
Our clean room and associated QC facilities have been developed to provide a highly flexible environment that can adapt to the specific needs of your mammalian cell-based project.
Our technology systems are designed to utilise
protocols from discovery labs and scale these to
produce cells/proteins sufficient for preclinical and
early clinical studies, at high speed and tightly
controlled quality.
At the end of a production run, our aseptic filling
technologies produce batches ready for release by our
QP, thus providing you with ready access to
downstream applications.
Our activities focus on supporting the transfer or our early stage discovery of GLP/GMP complaint production settings
our QC facilities are modifiable to your needs alongside our scalable cell cultivation protocols provide high-quality, repeatable batches
Our team will support you with your IMP application filings and ensure your projects meets regulatory standards
We work on cutting-edge Mammalian Cell research, across a range of R&D Projects.
We have recently completed production on our brand new state-of-the-art Clean Room Facility, with a highly flexible design to serve the needs of a wide range of mammalian cell-based technologies.
We still have a limited capacity to supply new partners, so please get in touch with your needs.
Effective communication, and support from an experienced management team that can help translate your project to full-scale production
Longstanding experience in mammalian cell technologies, with a special focus on primary stem cells.
Ensure high-quality standards with our ISO- certified environment and a well established documentation system.
Our dynamic Operations Team is led by Kata Dudas and includes highly experienced cell-culture researchers, regulatory experts and internal auditors of our GLP and GMP processes.
Our Broader Team includes a comprehensive suite of experts to meet the specific needs of our Partners. Delivery of your project is our top priority, please get in in touch and we will develop the optimal solution that meets your requirements.
“We received a great support from the Cellfactory Team throughout our R&D project and now are ready to test our stem cell treatment in regulatory clinical trials, to inform our marketing authorisation application in Europe and beyond. We could not wish for a more professional and highly effective yet, friendly team to work with!”