Devices (includes Medical Devices and In Vitro Diagnostics)
Olga van Grol-Lawlor, MPhil
Senior Global Regulatory Intelligence & Advocacy Manager
Boston Scientific, Netherlands
Daniel Caños, PhD, MPH
Director, Office of Clinical Evidence and Analysis, Office of Product Evaluation and Quality, CDRH
US Food and Drug Administration
Heather M. Colvin, MPP
Director, Evidence & Outcomes Policy
Johnson & Johnson MedTech
Sabina L. Hoekstra -van den Bosch, PharmD FRAPS
Global Director Regulatory Strategy
TÜV SÜD Medical Health Services, Netherlands
Monika McDole-Russell, MS, RAC
Sr. Director, Global Regulatory Affairs
Medtronic Endoscopy