Medico-Legal Expert Witness
TUV SUD
Hampshire, England, United Kingdom
Expertise in regulatory clinical affairs and medico-legal clinical negligence, supported by a robust background as a Consultant Neurosurgeon spanning more than a decade. Core competencies include EU MDR and UK MDR compliance, with significant contributions in developing new regulatory pathways for medical devices. Collaborative efforts include roles with the EU COMBINE project, Avicenna Alliance, Virtual Human Twin (EDITH) and BRIDGE (IHI). Regulatory and clinical expertise in orphan medical devices, In Silico methodologies and breakthrough innovative medical devices.
Widely recognized for advocating advancements in medical device regulation, driving impactful initiatives and authored white papers providing a Notified Body’s perspective on approval processes. Expertise in medical law complements clinical and regulatory work, promoting ethical and legally sound healthcare practices.
In Silico: Virtual Patients, Real Evidence: The Current Use of In Silico Regulatory Evidence
Thursday, May 7, 2026
12:00 - 13:00 WEST