Policies and procedures

To help ensure robust document management, we use Q-Pulse to securely store, review, and update quality documents.

Our Standard Operating Procedures (SOPs) and policies for the Experimental Medicine Facility and Clinical Trials Facility are managed by our Quality Assurance Manager in line with Good Clinical Practice (GCP) guidelines.

You can find some of these documents below, but please get in touch if you need additional documents or advice.

Please note quality documents for the Cell Therapy Unit (CTU) are managed by CTU Quality Director, Penny Bligh, in line with Good Manufacturing Practice (GMP) guidelines.