Explore the significance of ISO/IEC 42001 in promoting responsible AI use. Learn about key requirements and compliance steps.
Explore the regulatory frameworks, challenges, and best practices for post-market surveillance and maintenance of medical devices in the EU and US.
Explore the transformative impact of Artificial Intelligence in the medical device field, from disease detection to personalized treatment.
Learn about the qualification process, classification rules, and standards that apply. Stay compliant with medical device regulations.
New FDA's guidance providing updates on the documentation recommended for inclusion in premarket submissions for its review of device software.
