Welcome to the CEBR Webinar, organised in collaboration with the European Medicines Agency (EMA): “Regulatory Support Tools for Innovative Medicines and Technologies Developers”.
The free webinar will take place on November 26, 2025 at 10:00–11:30 CET.
This session will provide valuable insights into the regulatory tools and resources available at the EMA to support the development of innovative medicines and technologies in Europe.
You will hear directly from two distinguished speakers:
Hélène Casaert, Scientific Officer, EMA
Hélène is a pharmacist specialised in EU medicines regulation. With experience in regulatory affairs in the pharmaceutical industry and at the French national competent authority, she has been part of the EMA since 2015, supporting SMEs through the Agency’s SME Office and fostering innovation across the sector.
Sebastian Asprella, Programme Lead, EMA
With a multidisciplinary background in electromechanics, psychology and business, Sebastian brings extensive cross-sector experience spanning IT, space & defence, and life sciences. At the EMA, he leads initiatives aimed at strengthening Europe’s competitiveness by enabling predictable, science-based regulatory pathways that help clusters, tech-transfer offices and SMEs bring European science to patients.