LISAvienna cordially invites you to attend the 10th Regulatory Affairs Conference for Medical Devices and In-vitro Diagnostics, taking place on October 15, 2026, in Vienna. Expect a full day of presentations, interactive discussions, and practical insights covering all aspects of market authorization, including the latest updates on MDR, IVDR, and other relevant regulatory developments. The conference offers the opportunity to stay up to date with regulatory requirements while expanding your professional network, and facilitates learning from experts.

Preliminary agenda:

- Regulatory update

- Bridging regulation and reality: AI in medical devices under MDR and additional regulations

- EUDAMED: Insights from theory to implementation

- MDR/IVDR basics and market access know-how for start-ups to increase investment readiness

- Turning regulation into opportunity: MDR/IVDR revision for a resilient, secure and competitive European medtech sector

- International market access: Strategic considerations and proven success stories

- MDR inspections and audits: Learning from the regulator’s, notified body’s, and industry’s perspectives

- Regulatory workflow transformation in notified bodies and companies: How to reduce complexity and boost efficiency

- IVDR: Regulatory deep dive, practical insights and key considerations for in-house IVD

- Experts’ Corner: NIS2, reimbursement and clinical trial norms and standards

The conference will again be held in English. Strategic networking will be further supported by b2match, a professional partnering tool particularly valuable for start-ups and first-time participants. Early bird rates are granted until 6.8.2026.

Additional information is provided here: https://www.b2match.com/e/lisavienna-reg26/

15.10.2026, 9-18 Uhr

Apothekertrakt, Schloss Schönbrunn: Meidlinger Tor, Grünbergstraße | 1130 Vienna, Austria