Medical Device Software Webinar Series - Part 4: Integrating Clinical Needs into Design & Documentation
Date
Thursday, October 17th 2024 (16:00 - 17:00)
Price
€0 for non-members
€0 for members
Language
English
Organised by
QbD Group
Categories
Tags
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 demonstrate the safety, performance and benefits of your medical device software under the MDR?
In our 4th webinar, we'll explore the essential clinical evidence needed for success, including investigations, literature reviews, technical performance, and the use of similar devices.
We’ll discuss the critical role of clinical validation starting from the design phase and guide you on how to compile the necessary evidence to meet MDR requirements.
By attending, you’ll learn how to ensure your software not only achieves market access but also upholds patient safety and delivers effective healthcare outcomes.