About this webinar
What to expect.
Globally, medical device regulators are raising the bar. In Europe, a complex web of new and shifting regulations is creating a "perfect storm" for manufacturers and hospital operators. Are you prepared to make the right regulatory decisions?
Join experts from the Johner Institut and Medcrypt for a deep-dive session designed to bring clarity to complexity. We will decode the evolving EU ecosystem and show you how to build a precise, concise compliance strategy.
What We’ll Cover: 🇪🇺 The Interconnected Ecosystem: How MDR/IVDR updates, the CRA, and NIS-2 affect your software. 🤖 The AI Act: Navigating the specific requirements for AI-enabled medical devices. ⚖️ Strategic Decision-Making: Why a "precise yet concise" approach is your best defense against non-compliance.
