Join this to learn more about the regulatory tools and resources available at the EMA to support the development of innovative medicines and technologies in Europe.

You’ll hear from two key speakers from the EMA who will share their expertise and insights: 

Hélène Casaert, Scientific Officer, EMA

Hélène is a pharmacist specialised in the regulation of medicines in the EU. She has worked as a Regulatory Affairs Manager in the pharmaceutical industry and in the clinical trials sector at the French national competent authority. Since joining the EMA in 2015, she has been working as a Scientific Officer within the SME Office, providing dedicated support to SMEs developing medicines in the EU and driving innovation across the sector. 

Sebastian Asprella, Programme Lead, EMA

Sebastian has an academic background in electromechanics, psychology and business, and professional experience across IT, business, space & defence, and life sciences. He has delivered 19 products, managed €52M annually, co-led €100M+ IT implementations and teams of 130+ FTE.

At the EMA, he leads EU competitiveness, focusing on predictable, science-based regulatory pathways that help clusters, tech-transfer offices and SMEs translate European science into patient benefit. 

We look forward to seeing you there!