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Experience rapid transition from R&D to GMP-compliant production & EMA-approval of mammalian cells, stem cells, cell-based therapies, and biopharmaceuticals.
With decades of experience in culturing primary mammalian cells, a team of specialist scientists and QA experts, and GMP-compliant & ISO-certified facilities in the heart of the EU, Cellfactory is here 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 of your early stage discovery into full GLP/GMP complaint production settings
Our QC facilities are modifiable to your needs, while our scalable cell cultivation protocols ensure high-quality, repeatable batches
Our experienced team will support you with your IMP application filings and ensure your projects meets regulatory standards
Every single day, we’re work on various cutting-edge mammalian cell research, development, scaling, or manufacturing projects, across a wide range of clients.
We’ve recently completed the ISO-certification of our newest state-of-the-art clean room facility, with a highly flexible design. This ensures we can serve your needs, regardless of the specific mammalian cell-based technologies you require.
Due to exceptional demand, we only have limited capacity to work with new partners. So, if you’re interested in taking advantage of Cellfactory’s expertise, please get in touch as soon as possible.
Effective communication, and support from an experienced team of scientists who can help translate your biotech project to full-scale production
Longstanding experience in mammalian cell technologies, with a special focus on primary stem cells.
Ensure high-quality standards without the administrative headaches, with our ISO-certified environment and 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 – including scientists, quality control professionals, and more – to meet your specific needs. Delivery of your project is our top priority, please get in in touch to discover the best solution that meets your project’s 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!”