Sponsored Presentation: Regulatory Intelligence: From Information Overload to Strategic Decision-Making

Description: With a rapidly increasing pace of innovation in medical device development, regulatory teams need help keeping up with global regulatory frameworks and standards changes. However, with a modern regulatory intelligence (RI) program, Medtech organizations can proactively manage new regulations and provide strategic input to product development and quality. In this session, MedTech thought leaders will explore the critical processes and tools regulatory affairs needs to establish a successful regulatory intelligence program. They’ll share best practices for managing requirements without missing out on new information, how to alleviate the administrative burden of day-to-day activities and strategies for sustaining a regulatory intelligence program over the long term. Additionally, this session will include practical takeaways to help attendees start discussions with leadership on how to develop, support, and launch an RI program in their organization.