Medical Device Software Webinar Series - Part 3: A unified MDSW development cycle that covers all requirements
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.
Struggling with the complexities of Medical Device Software (MDSW) development? Need clarity on complying with standards like IEC 62304, IEC 82304, IEC 62366, and ensuring robust cybersecurity?
Our 3rd webinar of the series will explore the specific requirements for various safety classifications and provide valuable insights into what Notified Bodies (NBs) and the FDA expect from your development process.
Key topics will include the full development cycle, cybersecurity essentials, usability engineering, AI integration, and effective strategies for aligning agile methodologies with the strict release flows required for MDSW.
Gain a deeper understanding and streamline your MDSW development process!