The Cell production unit is a functional service that meets all the requirements stipulated by law for the manufacture of cell products for clinical research in compliance with Good Manufacturing Practice (GMP) standards. The unit was accredited by the Spanish Agency of Medicines and Medical Devices in 2009. It was audited in 2012 and certified again for its compliance with good manufacture practices.

The unit focuses in the manufacturing of mesenchymal cells, both autologous and allogeneic, to be used in humans, either through clinical trials or a compassionate use programme. Current therapeutic applications are focusing on the treatment of haematological disorders and patients with different osteoarticular, vascular, lung and autoimmune disorders.