Unlock the power of Glooko for your clinical trials

From clinical trials to real-world studies, Glooko partners with life sciences organizations for end-to-end clinical evidence development.

With Glooko as your strategic partner, life sciences organizations can bring diabetes treatments and technologies to market faster, more efficiently, and with greater confidence.

Benefits of partnering with Glooko:

  • Increase usage of connected products in decentralized and hybrid clinical trials due to demand for remote data collection and virtual visits
  • Leverage Glooko’s 21 CFR Part 11 compliant clinical trial platform for study data acquisition
  • Remotely capture granular real-world data in nearly real time
  • Easily manage multiple diabetes and health monitoring devices used in clinical trials
  • Simplify protocols for patients and increase adherence rates
  • Efficiently screen and recruit patients
  • Data tokenization to unlock a richer, longitudinal view of patient journeys without compromising individual privacy

Achieve success at every step of a clinical trial with Glooko

Our real-world data capabilities along with our comprehensive trial and data management platforms empowers life sciences organizations to make faster, scalable decisions across the clinical development lifecycle

Protocol Design

Use Glooko’s real-world data from more than 8,000 clinics to help select devices and determine protocol feasibility

Clinical Trial Site Selection & Patient Recruitment

Our real-world data and recruitment tools reveal where your target populations are and how they behave, enabling optimized site selection and precise patient identification to accelerate enrollment and improve clinical trial success.

Data Collection

Continuously collect data remotely in near real time and share with study sponsor throughout trials when patients can’t visit a clinic

Patient Monitoring & Study Management

Remotely monitor patients to ensure they are on track and view site performance via easy-to-use and nearly real-time dashboards

Data Export

Easily export data in a variety of formats for analysis

Protocol Design

Use Glooko’s real-world data from more than 8,000 clinics to help select devices and determine protocol feasibility

Clinical Trial Site Selection & Patient Recruitment

Our real-world data and recruitment tools reveal where your target populations are and how they behave, enabling optimized site selection and precise patient identification to accelerate enrollment and improve clinical trial success.

Data Collection

Continuously collect data remotely in near real time and share with study sponsor throughout trials when patients can’t visit a clinic

Patient Monitoring & Study Management

Remotely monitor patients to ensure they are on track and view site performance via easy-to-use and nearly real-time dashboards

Data Export

Easily export data in a variety of formats for analysis

Life Science Partners

At Glooko, we partner with leading life sciences companies to harness the full potential of real-world device data and drive faster, smarter decisions across clinical development. Our data can help reveal where target populations are and how they behave, accelerating recruitment and optimizing site selection. By linking real-world, clinical, and lab data through tokenization, we deliver deeper, privacy-safe insights into patient journeys to help bring diabetes treatments to market more efficiently and confidently.

Unmatched source for
real-world data

  • From acquisition to viewing, visualization, and export, Glooko is an unmatched source for real-world data from patients living with diabetes around the world.
  • 100B+ health data points from 30 countries and 20 languages
  • Robust datasets available, including glucose, insulin, exercise, food, and medications
  • Support for more than 200 diabetes and health monitoring, including BGMs, CGMs, insulin pens, smart scales, and fitness trackers, supported devices with provisioning available
  • Real-time data sharing with sponsors during the study
  • Compliant with HIPAA, GDPR, ISO 13485, and 21 CFR Part 11