AdvaMed is proud to host the Medical Device Submissions Workshops: 510(k) and De Novo in February 3-4, 2025! Choose to attend virtually or in person at AdvaMed’s Washington, D.C. office, where FDA officials and industry experts will provide essential guidance through the 510(k) and De Novo submission processes. Understanding the IDE process from start to finish will help reduce errors and ensure compliance with all FDA requirements. By attending this in-depth workshop, medtech professionals are better equipped to meet regulatory demands and bring their devices to market faster.
Join us to get your questions answered, discuss specific challenges, and gain expert insights into the 510(k) and De Novo application requirements to gain a deeper understanding of this essential regulatory pathway. Don’t miss this opportunity to enhance your regulatory knowledge and connect with your fellow regulatory peers!