Study services & tools

We work to realize your vision from the ground up, including trial design, operations, and analytics

From traditional site-based studies to hybrid and remote trials–clinical trials aren't one-size-fits-all. It all starts with unified technology that's simple and intuitive for sponsors, sites, and participants. Standardizing on one flexible foundation for trial operations–including software and strategic services–reduces complexity. Here's how we make it happen:

End-to-end solution

A connected platform that streamlines clinical operations from beginning to end, with role-based applications for sponsors, sites, and participants

Patient-focused design

Leveraging Google's best-in-class consumer technology design principles for a superior participant-centric experience

Advisory services and execution

We help accelerate your move to decentralized research by helping design and run your study

Participant engagement, data, and management

Simplify study management and digital evidence generation with connected, easy-to-use tools for participants and clinical operations managers

eConsent and document signing

Simple management of informed consent records with fully 21 CFR Part 11-compliant eSignatures. Study coordinators can release, co-sign, and view status with one click

Study tasks, ePROs, and surveys

Configurable study workflows and activities–designed for a digital-first, participant-centric world–reduce the burdens of manual processes

Virtual and in-home visits

Meet your participants where they are, through video calls or home health visits with licensed clinicians. Schedule and manage visits directly in the platform

Site tools

You don't need a bigger clinical stack: you need a single source of truth for your clinical data, and more coordinated operations. Modernize your approach and speed development timelines

eSource

An electronic source of truth is the foundation of faster, more trusted, and complete clinical data and documentation

Real-time dashboards

Role-based views of recruitment and study progress metrics for principal investigators and study coordinators

Sponsor tools

Our expert services team partners with you on trial design and delivers fully configured studies. Get up and running in weeks, not months, and leverage our world-class algorithms to activate your data

Real-time site monitoring

Compare key performance metrics across all sites in a single view

Data analysis

Turn your data into a competitive advantage. With powerful, proprietary algorithms and in-house molecular, data science, and biostatistics teams, we can help you generate more unique insights

Featured stories

Verily Study Watch

Verily Study Watch is a sensor-based wearable device for non-invasive, continuous monitoring.

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DCRI, Verily, and HERO Registry to Support Long-Term Safety Study of COVID-19 Vaccine

Verily is partnering with Pfizer and the Duke Clinical Research Institute (DCRI) on a long-term surveillance study...

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