11.45am – 12pm GMT, 6 November 2024 ‐ 15 mins
Presentation
Session One: The UK as a global attractive destination for clinical trials
Session Chair: Dr Martin O’Kane, Regional Head Regulatory Affairs EU Policy & Liaison, Novartis, and Member, BIA Regulatory Affairs Advisory Committee
Regional Head of Regulatory Affairs EU Policy & Liaison, Novartis Pharmaceuticals
Professor of Otology and Skull Base Surgery, University of Cambridge
Regional Head of Regulatory Affairs EU Policy & Liaison, Novartis Pharmaceuticals
Martin O’Kane PhD is Regional Head of Regulatory Affairs EU Policy & Liaison at Novartis Pharmaceuticals, responsible for developing and implementing complex regulatory strategies in global development and enabling regulatory compliance. He is co-chair of the European Federation of Pharmaceutical Industries Associations (EFPIA) Clinical Trials Regulation Pillar and is a member of the BIA Regulatory Affairs Advisory Committee. Martin has seventeen years’ previous experience in medicines regulation working in the Medicines and Healthcare products Regulatory Agency (MHRA), the majority of which was in the clinical trials field including scientific assessment of trial applications and development of policy, guidance, and legislation relevant to the UK’s exit from the EU and the UK response to COVID-19.Professor of Otology and Skull Base Surgery, University of Cambridge
Professor Bance is the Professor of Otology and Skull Base Surgery at the University of Cambridge. Prior to 2017, he was Chair of the Dept of Otolaryngology, Dalhousie University in Canada. He is a surgeon-scientist, who runs a basic science lab. He also runs a genetic hearing loss clinic, and has been involved with first in human studies for gene therapy for hearing loss