Generative AI to Propel RegTech into the Future

The medical devices industry is witnessing a transformative shift with the emergence of Generative AI and its numerous applications in Quality Assurance & Regulatory Affairs (QARA). Generative AI is rapidly becoming a cornerstone in RegTech, offering innovative solutions that enhance compliance, optimize Quality Management Systems (QMS), and address critical evolving challenges such as PFAS mitigation.

This virtual panel discussion brings together thought leaders to explore how Generative AI is revolutionizing medical device regulatory processes. Our experts provide deep insights into leveraging AI for gap assessments, post-market surveillance (PMS), complaints handling, and clinical evaluations. You will learn practical strategies to integrate AI-driven RegTech solutions into their compliance frameworks, ensuring both regulatory adherence and operational efficiency.

Watch to:

• Discover how Generative AI is driving advancements in QARA, streamlining compliance with the EU AI Act, and setting new standards for healthcare compliance.
• Learn how AI can enhance Quality Management Systems (QMS), improving transparency, efficiency, and risk management within regulatory processes.
• Understand how AI is revolutionizing post-market surveillance (PMS) and complaints handling, ensuring timely, accurate, and compliant reporting in the medical devices industry.