Update: Medizinprodukte & IVD
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LISAvienna Regulatory Conference - 10th anniversary!
On October 15, 2026, we celebrated the tenth LISAvienna Regulatory Affairs Conference on Medical Devices and In Vitro Diagnostics in Vienna! As a longstanding partner, we are thankful for our partnership and the active community in Austria....
Why book seminars now? Because regulatory knowledge cannot wait.
The MDR, IVDR, EUDAMED, the AI Act, and new technical requirements are constantly evolving. Training today helps avoid costly delays, documentation gaps, and market access risks tomorrow.
Build your expertise now, before requirements becom...
Vortragsunterlagen: Regulatory Update Revision MDR, IVDR, EU-AI Act und Schwachstellen Techn. Doku vom 16.09.2026
Am 16.09.2026 fand unser regelmäßiges Online-Forum: Regulatory Update gemeinsam mit den Life Science Clustern aller österreichischen Bundesländer statt.
Rund 50 Interessierte waren bei den Updates der Expert:innen und den Best-Practice-Vor...
Online-Forum Roundtable: Regulatory Update für Medizinprodukte und IVD am 16.09.2026
Zusammen mit den Life Science Cluster Organisationen Standortagentur Tirol , LISAvienna , Human.technology Styria GmbH , Medizintechnik-Cluster Oberösterreich, ecoplus. Niederösterreichs Wirtschaftsagentur GmbH und Innovation Salzburg...
Regulatory Update für Medical Devices & IVD: Wissen, das Sie jetzt brauchen!
MDR, IVDR, Medical Software und AI-based Medical Devices stellen Unternehmen vor immer komplexere Anforderungen. Unsere en.co.tec Certificate Courses vermitteln praxisnahes Know-how, aktuelle regulatorische Entwicklungen und direkt anwendba...
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