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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.
United States