TRIALS CONNECT PEOPLE TO POSSIBILITIES
Clinical research, connected.
Databean combines clinical research expertise with TrialPoint™ technology to connect the people, workflows, data, and insights required to design, execute, and oversee clinical research.
From study design through execution and evidence generation, we bring the expertise and technology together so your team can see what’s happening, act sooner, and keep research moving.
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EXPERTISE TO MOVE YOUR STUDY FORWARD. TECHNOLOGY TO KEEP IT CONNECTED.
Embedded partnership
We work as an extension of your team, connecting sponsors, CROs, institutions, clinicians, and vendors to keep technology, people, and processes aligned.
Technology-enabled execution
Purpose-built technology configured around your processes, protocol, workflows, regulatory requirements, and users—supporting efficient execution from study start through closeout.
Quality without compromise
Quality, compliance, and traceability are built into every workflow from the start—not layered on at the end.
Why connect your study?
Clinical studies generate vast amounts of information across sponsors, sites, systems, vendors, and external teams. When that information is fragmented, study leaders spend too much time assembling the picture instead of using it to make informed, timely decisions.
A connected study brings clinical and operational activity together, making it easier to see relationships, identify emerging issues, and understand what is happening across each study.
Enrollment + Site Performance
Go beyond enrollment numbers to understand where performance is changing, which sites are driving results, and where attention may be needed.
Monitoring + Clinical Data
Use current study data to identify emerging risks, focus oversight, and determine where timely intervention may be needed.
Safety + Clinical Events
Connect safety and clinical events with the underlying data, documentation, and review needed to understand context, support decisions, and maintain traceability.
Investigational Product
Maintain complete product accountability by connecting inventory and product activity directly to the subjects, sites, and visits associated with its use.
Documents + Study Execution
Keep essential documents and quality records connected to the study activities, workflows, and decisions that generate them—improving traceability, accountability, and inspection readiness.
Data + Decisions
Turn study information into actionable dashboards and insights that help teams identify emerging trends, prioritize attention, and make informed decisions.
That’s the difference between simply collecting study information and using it to understand what is happening across your study.
Meet TrialPoint™
One Platform. Your Entire Study. Connected.
TrialPoint™ is Databean’s configurable clinical research platform, bringing together the applications, workflows, data, documents, and insights needed to manage and execute research within one connected environment.
Configure TrialPoint™ applications to meet the needs of each program while maintaining a consistent, connected environment across your entire research portfolio—without the complexity of deploying and managing separate systems for every study.
Examples of supported programs and studies include:
eTMF & Quality
Connect essential documents, training, quality processes, and compliance records directly to the study activities, workflows, and people they support—creating clear accountability and end-to-end traceability.
Documents in context.
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Study Management & Monitoring
Connect sites, subjects, milestones, monitoring, issues, workflows, and study activities in one operational environment for greater visibility, coordination, and control.
Keep execution visible.
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EDC
Capture, manage, review, and report clinical data within TrialPoint™, keeping data connected to study operations, workflows, and oversight.
Clinical data in context.
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Safety & CEC
Manage safety and clinical events within TrialPoint™, connecting source data, supporting documentation, medical review, decisions, and adjudication in a traceable workflow.
Structured review. Complete traceability.
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IP Accountability
Maintain end-to-end investigational product accountability across shipment, receipt, inventory, assignment, use, return, and reconciliation—with clear visibility and traceability throughout the study.
Know where every product is.
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Reporting & Dashboards
See enrollment, site performance, monitoring, data quality, safety, quality, milestones, and risk in one connected view—without manually assembling information across systems.
Turn study activity into insight.
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Why Databean?
Clinical experience built the technology.
Since 2007, Databean has helped organizations design and conduct clinical research across complex development programs.
That experience also exposed a persistent problem: the technology supporting clinical research was often disconnected from the way studies actually operate.
So we built TrialPoint™.
Today, Databean’s clinical and technology teams work as one. Clinical experience shapes how TrialPoint™ is designed and configured, while TrialPoint™ gives our teams and clients better ways to execute, oversee, and understand their studies.
Databean brings the expertise. TrialPoint™ connects the work.
Learn About Databean
Real-world experience.
A more connected way to do research.
People. Process. Technology. Better outcomes.
Years of Experience
17+
Supporting clinical development since 2007.
Expertise in Action
100+
Studies designed, implemented, and supported.
A More Connected Way
1 Platform
Clinical services and technology working together.