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Company History
1997
- Founded as a spin-off from the Idar-Oberstein based Bone Marrow Transplantation Unit
1999
- Granted a first Manufacturing licence from the local authorities for the production of bone marrow and apheresis stem cell products as well as cord blood preparations
- Since then manufacturing and quality control of stem cell products (bone marrow, apheresis, cord blood)
2000
- Manufacturing licence is extended to cover the production of diverse retroviral vectors and genetically modified CD34+ stem cells
2001
- EUFETS becomes a subsidiary of Fresenius Biotech GmbH
- EUFETS decides to build new clean room facility
- Manufacturing licence is extended to cover the production of diverse retroviral vectors and genetically modified T-cells
2002
- EUFETS supports first clinical trial with retroviral vector and allogeneic gene-modified T-cells (suicide gene therapy)
- EUFETS performs first GLP studies
2003
- EUFETS achieves accreditation as Good Laboratory Practice (GLP) facility
- New production facility is inspected and accepted by the local authorities for the production of cell- and gene therapy medicinal products
- EUFETS produces retroviral vector for ADA SCID gene therapy trial in UK
2004
- Manufacturing licence is extended to cover the production of genetically modified HIV+ T-cells as well as several new retroviral vectors
- EUFETS produces study medication for a phase I/II anti HIV gene therapy (autologous T-cell) trial
- EUFETS produces gene-modified autologous stem cells for a phase I/II CGD gene therapy trial
- EUFETS produces retroviral vector for several clinical gene therapy trials in Europe
2005
- New large scale GMP production technique for retroviral vectors and subsequent concentration is established and validated
- Manufacturing licence is extended to cover the new production techniques for retroviral vector production
- EUFETS produces retroviral vector for several clinical gene therapy trials in Europe and Japan


