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Advancing Medical Technology Research with Purpose-Built Expertise

Designed to Support MedTech Trials at Scale

Medical device and technology studies operate under a distinct set of demands. From IDE and PMA pathways to post-market clinical follow-up, usability endpoints, and real-world performance data, MedTech sponsors require a modern clinical research technology to sync with their innovative medical technology.

THREAD has partnered with MedTech sponsors and their CROs globally to design, operate, and scale clinical studies that reflect the unique regulatory, scientific, and operational complexity of device-focused research. We understand that MedTech trials are not simply adapted pharma protocols. They require a purpose-built approach, fit-for-purpose technology, and a partner with deep device study experience across the full product lifecycle.

Advancing Medical Technology Research with Purpose-Built Expertise

A Platform Built for the Complexity of Device Studies

THREAD's configurable, full-featured clinical research platform gives MedTech sponsors the technology infrastructure to capture the right data, at the right time, from the right source. Our integrated eConsent, eCOA and eSource solutions support the collection of clinician-reported, observer-reported, and patient-reported outcomes critical to device performance evaluation.

Virtual visit capabilities enable remote monitoring and follow-up assessments that reduce costs and site burden while maintaining protocol compliance. Seamless integrations with validated sensors, wearables, and digital health technologies allow sponsors to capture objective, device-adjacent performance data directly from participants in real-world settings to deliver complimentary evidence modern regulators and payers increasingly expect.

Advancing Medical Technology Research with Purpose-Built Expertise

Consulting Services Designed for the MedTech Patient Journey

THREAD's consulting team brings cross-functional expertise in MedTech study design, endpoint strategy, and global execution to every engagement. From early feasibility through post-market surveillance, our consultants work alongside MedTech sponsors and CROs to build study architectures that meet regulatory standards while optimizing efficiency, data quality, and participant experience.

Whether your study requires a site-based, hybrid, or fully decentralized approach, THREAD delivers the strategic guidance and global infrastructure to help MedTech companies run smarter, faster, and more inclusive clinical studies, bringing our customers' innovative technologies to the patients who need them.

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