Geoff Kitson has over 27 years experience from the pharmaceutical industry, and a broad-based international perspective on drug development, from phase I to phase IV, experience of pre-clinical work, and regulatory requirements. He has been involved in the preparation of INDs, CTXs/CTAs, MAAs and other regulatory documents. He has experience in the development of individual clinical studies, clinical trial programmes, multinational clinical trials and developing clinical strategies. In the last few years he has taken 5 products including 5 vaccines through to first in man studies, and progressed products through to Phase II/III.