David Sudworth

David Sudworth is a seasoned regulatory professional with extensive experience in the pharmaceutical industry. Currently serving as Principal Regulatory Consultant at DLRC Regulatory Consultancy since December 2019, Sudworth has previously held senior roles at Mylan as Senior Director of Regulatory Affairs, where responsibilities included ANDA and NDA approvals, BLA submissions, and management of regulatory agency interactions worldwide. Prior experience at Pfizer included positions such as Regulatory Team Manager and Clinical Protocol Lead, overseeing product development and clinical operations across numerous trials in gynaecology and urology. Sudworth's educational background includes an MSc in Pharmaceutical Medicine from the University of Surrey and a BSc in Genetics from Swansea University.