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Step 7:

Analysis & Reporting

From Raw Data to Real-Time Insight—
All in One Platform

Un ensayo clínico es tan valioso como la fiabilidad de sus resultados. Los expertos en DCT de ObvioHealth saben cómo diseñar un ensayo para reclutar y capacitar a la cohorte óptima y eliminar el «ruido» estadístico, de modo que puedas obtener las pruebas sólidas que necesitas.

Customizable Analytics at Your Fingertips

No more waiting on static reports or disconnected tools. ObvioGo’s customizable dashboards let teams track study trends, participant activity, and operational milestones in real time. Slice data by site, cohort, or task status—and surface exactly what you need, when you need it.

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Selección y validación de instrumentos

With ObvioGo’s AI Assist, users can quickly uncover patterns, detect anomalies, and locate subsets of interest.
Whether identifying safety signals or monitoring site performance, the platform helps surface what matters—
fast and intuitively.

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Seleccione los instrumentos óptimos

Identificamos los instrumentos, dispositivos y dispositivos portátiles que son más apropiados para la población, la afección y el tratamiento en estudio.
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Evalúe las ventajas y desventajas

Arbitramos entre la reducción de la carga de los pacientes y la calidad de los resultados, teniendo en cuenta la fatiga, la usabilidad y la granularidad de los datos.
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Proactive Risk Detection

The platform detects anomalies or outliers in participant data, enabling earlier intervention and improving safety oversight throughout the study.

Stay Ahead with Real-Time Task Tracking

The platform’s built-in task engine provides visibility into operational progress at both the site and participant levels. Whether it’s pending assessments, overdue follow-ups, or site-level alerts, teams can easily prioritize and reallocate resources to stay on track

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Operational Milestone Tracking

Get real-time visibility into task status across participants and sites—whether it’s missed assessments, overdue follow-ups, or incomplete data submissions. ObvioGo makes it easy to stay ahead of potential delays.
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Prioritization & Resource Allocation

Intelligent task dashboards help study teams and site coordinators identify bottlenecks and reallocate effort where it’s needed most, improving trial efficiency and site engagement.
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Workflow Transparency Across Teams

From CRAs to site staff to study leads, every stakeholder has access to role-based views of operational progress. This shared visibility supports smoother collaboration and faster resolution of site-level alerts.

Centralized Oversight for Sponsors

Sponsors and study leads access centralized dashboards that track protocol adherence, site performance, and participant engagement. Dashboards are configurable for interim reviews, stakeholder updates, or executive summaries. These features give sponsors stronger oversight—and with fewer dropouts and cleaner, real-time data, they gain stronger evidence, faster.

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Cross-Site Benchmarking

Compare site performance, enrollment rates, and task completion across locations to identify trends and outliers.
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Stakeholder Reporting Made Simple

Export interim summaries and visuals to support reviews, governance meetings, or sponsor updates.
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Strategic Oversight

Gain a top-down view of trial health without diving into raw data—perfect for executive monitoring and decision-making.

Audit-Ready Reporting

Every report is backed by time-stamped logs, role-based access controls, and exportable datasets—meeting 21 CFR Part 11, ICH-GCP, and other global compliance standards. Automated workflows streamline inspection prep and reduce last-minute scrambles.

Why It Works

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Seamless Trial Oversight from One Platform

ObvioGo unifies data capture, monitoring, and reporting in one environment—reducing integration risk, minimizing manual reconciliation, and streamlining GCP-compliant oversight from first patient in to database lock.
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Accelerated Decision-Making for Trial Teams

Real-time alerts and role-based dashboards help study teams detect issues early—whether it's a lagging site, missed visit, or emerging safety trend—so they can take action before problems escalate.
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Inspection-Ready by Design

From time-stamped logs to access-level audit trails, every action is documented to meet 21 CFR Part 11 and ICH-GCP. Data exports and reporting workflows reduce last-minute scramble for inspections and interim reviews.
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Making Real Impact

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