Join Lindus Health, Glucotrack, and Motif Neurotech for a deep-dive into the most common pitfalls that traditional Contract Research Organizations (CROs) make when running medical device trials—and what you can do differently.

In this insightful session, our experts unpack why standard approaches often fall short when applied to devices, from misaligned operational models to poor logistics and regulatory planning. Discover how forward-thinking trial design, sharp regulatory insight, patient-centric recruitment, and integrated tech can accelerate timelines and deliver stronger outcomes for your device studies. Whether you’re a sponsor, researcher, or investor, this live panel discussion will challenge outdated norms and equip you with practical strategies to run smarter, faster, and more effective medical device research.

• Meri Beckwith (Co-founder, Lindus Health)
• Paul Goode (COO, Glucotrack)
• Julie Goode (VP Clinical Affairs, Motif Neurotech)