Jessica is the Head of Regulatory Affairs at LFH Regulatory. After achieving a BSc (Hons) in Biology at Queen Mary University of London, she completed an Internship in Project Management at a global pharmaceutical company, which is where her interest in medical devices and regulatory affairs started. Since then she has worked on a large variety of devices and worked on global registrations for Class I SaMD to Class III Implants, in small start-up organisations to large global companies.
The last few years she has specialised in regulatory strategy for software and digital health tools in global markets and the many ways in which software can be leveraged in healthcare; from data collection tools in drug development to their use in disease management and beyond.
