Implementing a Regulatory Information Management (RIM) system in MedTech can unlock significant efficiencies—but only if done right. This roundtable will explore common missteps that derail RIM initiatives, including relying on solutions—whether commercial or homegrown—that aren’t purpose-built for the unique needs of MedTech, and insufficient executive sponsorship to drive necessary internal process changes. Participants will share real-world experiences, lessons learned, and strategies to boost user adoption during RIM rollouts. Join the facilitated discussion to strengthen your implementation roadmap and set your organization up for success.
Learning Objectives:
Identify why some RIM systems often fail to meet MedTech-specific needs.
Understand the critical role of executive sponsorship in achieving process harmonization.
Explore practical approaches to boost user adoption and engagement during RIM rollouts.
