Medical Device Software Webinar Series - part 1: Overcoming Initial Obstacles in Medical Device Software Development
Are you developing software that impacts patient health?
This five-part webinar series is designed to guide manufacturers through the complexities of bringing Medical Device Software (MDSW) to market. Each session will cover crucial aspects from initial concept to regulatory compliance, ensuring your software meets all necessary standards for successful commercialization.
Led by industry experts, these webinars offer in-depth knowledge, practical examples, and strategic advice, empowering you to navigate the regulatory landscape with confidence.
In the first webinar, we’ll address major challenges in software qualification and classification for different functionalities. We’ll explore MDR for software-hardware combinations and how AI is handled under the AI Act.
In addition, we’ll share essential resources, key standards, and guidance documents crucial for getting your product to market, from design and development to clinical evidence and technical documentation.
Ready to dive in?
Register here