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.
Schedule a DemoProven 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.
Learn More
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.
Learn More
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
-
Optimize Study Planning
Leverage industry data to identify high-performing research sites and centralize outreach and responses. Surveying sites in a centralized manner (versus fragmented processes like emails and other portals) enables sponsors and CROs to monitor and store real-time response rates and survey results, while minimizing burden and redundant data requests of sites.
-
Reduce Critical Path Cycle Times in Study Startup
Automate and streamline document collection, training, CDA execution by each stakeholder. Leveraging standardized approaches to study startup across your research portfolio reduces cycle time by minimizing duplicate tasks for sites and study teams. Enabling all stakeholders to achieve critical milestones in a compliant manner.
-
Guide Study Conduct
Ensure compliant and confident protocol execution by sites via innovative just-in-time study-specific training content and visit guidance. Working in a unified platform that guides the collection and approval of documents between sites, sponsors, CROs, and patients, and automates the flow of documents across their technology systems, will maximize time savings and improve compliance.
-
Oversee Study Progress
Increase visibility into study operations and identify areas of risk or potential intervention. View study status at the investigator, site, country, or regional level across your entire research portfolio, with intuitive next steps on how to communicate with those involved.
-
Audit-ready Study Closeout
Ensure accurate, readily available, and up-to-date trial master files (TMF) and investigator site files (ISF) via traceable integration to your eTMF.
Testimonials
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
4 Modernized Functions Every Sponsor Needs for Study Startup
This white paper outlines four technology capabilities sponsors need to expedite the study startup process.
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.
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.
