This event brings together regulatory, legal, and global regulatory agency perspectives to share strategies and methodologies on current challenges faced by medical device regulatory affairs teams working to secure product approval. Explore how your peers educate and engage internal stakeholders in clinical research/performance evaluation, quality assurance and post-market surveillance to gather and fulfill submission requirements in multiple global markets. Case studies and group discussions highlight practical experiences among shifting regulatory expectations. Foster a sense of collaboration and safely connect with peers and expert presenters at this intimately-sized program. Customize your experience and address your unique concerns during dynamic Q&A after each session. Our commitment to industry perspectives keeps the program focused on what matters and dynamic session types allow you to stay engaged.