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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