About Us
The isolation and characterisation of human stem cell lines is a complex process which applies many different technologies and is subject to rigorous regulatory and ethical control. Furthermore, to produce cell lines which are suitable for use in human clinical applications, they must be isolated, processed, stored and tested to current Good Manufacturing Practice (cGMP) standards.
Roslin Cells has been independently verified according to stringent standards and successfully attained ISO 9001:2008 certification in February 2009 (Certificate Number: FS 544151). Since then, the company have continued to demonstrate these meticulous standards, with successful annual renewals of their Human Tissue Authority (HTA) and Human Fertilisation and Embryology Authority (HFEA) licenses.
