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Steve qualified in biochemistry before completing a PhD and post-
He began his regulatory career with Smith & Nephew before moving to Chauvin Pharmaceuticals where he managed clinical research and drug safety functions in addition to the regulatory team.
In 1998 Steve joined Phoenix International to lead and develop the European regulatory group.
He went on to become Global Head of Regulatory Affairs and Drug Safety for MDS Pharma Services.
Steve’s regulatory expertise is focused on the clinical area, most notably in scientific advice, orphan drugs, paediatric investigation plans, development planning, elaboration of regulatory strategy and preparation of clinical overviews and summaries.
He is a regular trainer on clinical development topics for TOPRA and has also presented at numerous other symposia in Europe, US and Japan.