EU regulatory affairs editor
Amanda Maxwell is European Medtech Regulatory Affairs Editor at Medtech Insight.
She has some 30 years’ experience in reporting and providing analysis on developments in the field of medical technology regulatory affairs, with particular focus on the current and future EU regulations for medical devices, IVDs and device/drug combination products.
Amanda also has experience in providing medtech regulatory strategy consultancy services, and
is a frequently invited speaker and chair at EU meetings on medtech regulations
Tuesday, October 27, 2020
08:30 – 09:30 CET