Medical Device Software Webinar Series - Part 5: Technical Documentation Essentials for Medical Device Software
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 to create MDR-compliant technical documentation for your Medical Device Software?
In our last webinar of the series, you'll gain practical insights on crafting essential technical documentation with confidence.
We’ll take you step-by-step through interpreting MDR requirements, choosing the right accredited Notified Body, and navigating the qualification and classification process—all with a focus on your software’s Intended Purpose.
Don’t miss this opportunity to ensure your documentation is not just compliant, but also clear and comprehensive.