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Unified Trial Acceleration Platform

Your Clinical Command Center for Efficient and Compliant Research

Centralize research operations within Longboat globally for all sites, sponsors, and contract research organizations (CROs) to accelerate study startup, guide efficient and compliant study conduct, enhance patient outcomes, and streamline critical coordination.

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Proven Success

Unifying global researchers across 71 countries


Research personnel


Site users


Study participants

Key Platform Features

Secure Document Exchange

Accelerate study startup via end-to-end integration and automated, seamless exchange of research documents between sites, sponsors, and CROs.
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Safety Letter Management

Simply and effectively distribute safety reports to clinical investigators with visibility into status at the site, region, or global level across your clinical program.
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Learning Management System

Support site staff with study-specific training, including task- and event-based training deployment, assessment and certification, and oversight into training completion.

Site Feasibility

Gather critical information about potential site partners with a workflow tool to combine multiple site lists, route for review/approval, and track site status.

Site Engagement

Centralize engagement and oversight of site operations while providing intuitive resources for prescreening, consent, visit guidance, and visit calculations to increase compliance.

Patient Engagement

Support participants on their study journey from recruitment through to trial close-out with information and resources they need to be informed, compliant, and retained.


Global Oversight Dashboards and Analytics

Complete global visibility for real-time reporting across all site and patient activities assigned, in-progress, and completed on your trial

Why Longboat


What Study Teams Have to Say

As clinical trials increase in complexity and remote workflows, it is essential to have intuitive and centralized technology supporting our clinical operations. My work has made clear the value of easy access for sites to key study training, resources, communications, and visit guidance across our research portfolio.

– Medical Director, Parexel, Europe

What Site Users Have to Say

Document exchange has been a pain point for sites, often resulting in duplicative work and additional training burden for our staff who have to learn a different system for each sponsor. Giving our research teams the ability to leverage regulatory integrations to share documents with sponsors will be a game-changer, particularly during study startup.

– Associate Dean for Clinical Research, Duke University, United States

Read our Related Resources

White Paper

4 Modernized Functions Every Sponsor Needs for Study Startup

This white paper outlines four technology capabilities sponsors need to expedite the study startup process.

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White Paper

The ROI of Site-Centric Training and Support

Download our white paper to learn how to maximize your research investment for site-centric training and support.

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The Current State of Study Activation and Methods to Ensure Success

This webinar will discuss the importance of protocol feasibility and identifying solutions to ensure your organization's success.

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Visit the Resource Library

Informed by the Site-Sponsor Consortium

Advarra’s Site-Sponsor Consortium, made up of research site, sponsor, CRO, and data standards leaders, aims to make clinical trials smarter and more efficient by integrating clinical research site and sponsor technology.

Their input and philosophy are brought to life in the Longboat Platform achieving practical efficiencies across everyday workflows. In addition, its site-centric approach lays the foundation for processes that can be scaled across any vendor system.

Read the Press Release Read our Newsletter

Site-Sponsor Consortium