Regulatory Considerations for AI in MedTech

As artificial intelligence continues to revolutionize the medical technology industry, navigating the evolving regulatory landscape is crucial for success. This webinar will provide insights into key regulatory considerations for AI-driven medical devices, including FDA requirements, risk assessment, validation strategies, and emerging global regulatory trends.

Join Jennifer Palinchik and Fehmida Kapadia as they discuss best practices for bringing AI-powered MedTech innovations to market while ensuring safety, efficacy, and compliance. Whether you're a startup, an established MedTech company, or a regulatory professional, this session will equip you with the knowledge to navigate regulatory challenges effectively.