Join Lindus Health, Glucotrack and Motif Neurotech on June 24, 2025 as they dive into the recurring mistakes CROs make in medical device trials—leading to costly missteps and timeline delays—and reveal strategies for successful study execution.
Most contract research organisations (CROs) are much more well-versed in running drug trials than medical device trials.
As a result, they end up using these plug-and-play tactics to approach essential operations in device research—from flawed study design and logistical activities to inadequate monitoring and data collection practices.
The consequences? Low-quality study data, overspending, and time-consuming lags in getting your device to market. It’s about time we rewrite the narrative.
On June 24, 2025, Lindus Health will be hosting a FREE live panel discussion exploring how medical device researchers can steer clear of these missteps and drive innovation.
They’ll be joined by experts from Glucotrack and Motif Neurotech, who will share their firsthand experiences in working with CROs on medical device trials and where they felt their research was mismanaged.
There will also be time for a Q&A session to engage with panelists in real-time.
Logistical Discrepancies Between Medical Device and Drug Research
Many CROs don’t really “get” medical device trials.
In contrast to drug trials, medical device trials typically take longer to complete, require increased oversight of key functions, including patient monitoring and device production and handling.
These important distinctions require a nimble and informed research partner.
The Cost of Medical Device Research
Despite requiring fewer patients and shorter timelines, device trials don’t always cost less than pharmaceutical trials. Why? Many CROs price their services based on drug trial models—overcharging for unnecessary infrastructure and underdelivering on the services that matter. In this segment, panelists will discuss how they feel CROs are adapting pricing infrastructure for the realities of device development.
What Medical Device Researchers Actually Need
What does it take to run an efficient, high-quality medical device trial? Device development demands flexibility, responsiveness, and a deep understanding of regulatory and operational nuances. Discover the difference in working with a CRO with deep-rooted industry expertise.
Who Should Attend?
Whether you’re currently running a device trial or planning your first feasibility study, this session will help you build smarter development strategies that get your device to market faster and more efficiently.
Reserve Your Spot Today
You won’t want to miss this FREE opportunity to get candid, practical insights on CRO fit and function!
Register today to join us live or receive the on-demand recording.
Date: June 24, 2025
Time: 11:00 AM EDT / 8:00 AM PDT / 4:00 PM BST
Duration: 60 minutes
