Director, Medical Device Regulatory Affairs
Celegence
MSc RA, Medical devices with over two decades’ experience in medical device regulatory affairs specializing in lifecycle management of medical devices and IVDs ranging from research, design and development, regulatory submissions and approvals and post market surveillance. Therapeutic area expertise includes Diabetes, Ophthalmology, Nicotine Replacement Therapy (NRT), and Extracorporeal Membrane Oxygenation (ECMO).
Thursday, May 7, 2026
14:00 - 14:25 WEST