NoBoCap Panel at BEHEALTH 2025: Medical Devices Regulations (MDR and IVDR) – Impacts on Healthcare Systems
📅 21 October 2025 | Bucharest & Online
The NoBoCap Project will be featured in this year’s BEHEALTH 2025 International Event in Healthcare and Bioeconomy, through a dedicated panel exploring the impact of Medical Devices and In Vitro Diagnostic Regulations (MDR & IVDR) on healthcare systems, innovation, and market access.
The session – “Medical Devices Regulations (MDR and IVDR): Impacts on Healthcare Systems” – will bring together experts from across Europe to discuss how MDR and IVDR shape the future of MedTech, how innovation and compliance can work hand in hand, and what steps are needed to strengthen regulatory capacity for a resilient and innovation-friendly EU market.
Speakers:
- Başak Baranoğlu Demirci – Founder, AdviQual
- Petr Bratka – Head of Notified Body, Expert in Biocompatibility & AI
- Ruth Beckers – QA/RA Consultant Medical Devices, Qualix
- Miguel Amador – Chief Innovation Officer, Complear
- Liz Renzaglia – Domain Lead, MedTech & Digital Health, Biovia
- Yves Verboven – Founder, EU4HealthSolutions
- Flaviana Rotaru – President, ROHEALTH
The panel will be moderated by Mădălina Argăseală, Senior Expert, ROHEALTH, and will conclude with reflections from the NoBoCap consortium on how regional collaboration and Notified Body capacity-building can help accelerate CE-marking and support safer, more efficient innovation in Europe.
👉 Join us at BEHEALTH 2025 to take part in this important conversation on the future of MedTech regulation.
Register and schedule your meetings at: www.b2match.com/e/behealth-2025
