Tibor Zechmeister

Tibor is a medical technology specialist with 15 years of experience in the MedTech industry.

He has founded or co-founded several companies in the neurological medical device sector and was responsible for managing the entire regulatory approval process according to the MDD and MDR. Today, as Head of Regulatory & Quality at Flinn.ai, he oversees all regulatory corporate and product requirements, with a particular focus on the validation of Artificial Intelligence (AI).

In addition, Tibor acts as a Lead Auditor at a Notified Body, thereby combining entrepreneurial practice with deep, audit-verified regulatory expertise to bring safe and innovative medical devices to patients faster.

What matters most to him as a speaker:
“It is especially important to me that rapid innovation remains the driving force for real improvements in healthcare. Therefore, I not only advocate for full regulatory compliance but also pursue pragmatic approaches that enable efficient fulfillment of requirements and the swift market introduction of safe, life-saving medical devices.”