Ilona Őzse

I am Ilona Őzse, a quality engineer with more than a decade of professional experience in the field of medical devices.

Dorottya Lőrincz

I qualified as a chemist in 2003. I worked for almost 9 years in a manufacturing company where I was involved in product development, quality control, setting up the quality management system and regulatory affairs.

Stephanie Fossat – Dominguez

Stephanie has 17 years in the medical device industry, with recognized strength for enabling and managing change, empowering teams and managing metrics.

Michael Galliker

With over 15 years of expertise in the medical device industry, Michael Galliker has dedicated his career to mastering the complexities of regulatory affairs.

László Bódis

László Bódis is a highly accomplished professional with a diverse background in economics, innovation and policy.

Krisztián Szigeti

Krisztián Szigeti is a specialist in medical imaging, holding an MSc in biophysics and a PhD in pharmaceutical sciences from Eötvös Loránd University (2001) and Semmelweis University (2008), respectively.

Maurice Deuss

Maurice is responsible for the Business Unit Medical within PAYERGROUP, a multinational company supplying to ODM in the role of Contract Manucturer or OEM with production site in Austria, Hungary, China and Maleisia.

Michael Kania

Michael discovered the great need for digitalisation in medtech 14 years ago at Fresenius Kabi and found his passion in the field of regulatory affairs.

Dr. Christina Ziegenberg

Dr Christina Ziegenberg has a background in medical technology, the chemical industry and pharmacy, with a diploma as a chemist, a diploma in pharmacy from the University of Vienna and a doctorate from the Private University of Liechtenstein (UFL).

Tomasz Koeber

Long-time employee of the Polish Competent Authority, expert in the European Commission’s Twinning Project for the Medicines Agency in Moldova, in the field of medical devices.