This webinar will provide insights into the EU regulatory framework and practical considerations for the development and assessment of digital products and products combining medicinal products, medical devices and digital health components. The webinar will present complementary perspectives from the industry and a notified body.
The webinar will focus on:
• EU regulatory framework for the combined use of medicinal products, medical devices and digital health, including artificial intelligence
• Lessons learned from the Medical Devices and In Vitro Diagnostics Regulation for medical software development
• NB perspectives on software/AI assessment, including cybersecurity