Clinical Technologies Solutions
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TrialKit Engage For Televisits
12/29/2025
Conduct secure video based visits, manage study schedules, and keep participants connected through a single unified platform.
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Greenphire Clinical Finance: Budgeting & Benchmarking
10/23/2025
Streamline trial budgets and payments with real-time fair market data, speeding startups and ensuring timely, transparent site funding worldwide.
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Data Management
3/25/2026
In clinical research, data are everything. At inSeption Group, we understand the vital role data management plays in getting life-changing treatments to patients faster.
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IQVIA Feasibility
9/27/2022
Employing a digital, data-first strategy, IQVIA Feasibility brings together survey data, confidential disclosure agreements (CDAs) and site intelligence data, enabling sponsors to efficiently collect vital information while improving the site experience.
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Introducing Sitetrove Global Patient Insights
5/15/2024
With these insights, study sponsors can get a comprehensive view of the worldwide patient landscape, enabling the ability to locate sites with clinically relevant and diverse patient populations easily.
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Targeted Source Data Verification
2/6/2025
Ergomed’s Risk-Based Clinical Monitoring and Source Data Verification Approach for Data Integrity
Ergomed ensures the highest data integrity and patient safety standards through our risk-based clinical monitoring and Source Data Verification (SDV) practices. SDV is a critical process in clinical trials that ensures the data collected are accurate, complete, and verifiable against the source documents. We compare data entered into case report forms or electronic data capture systems with the source data to confirm their accuracy and reliability.
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Rave TSDV - Improve CRA Efficiency And Reduce Site Burden
1/5/2026
Source data verification (SDV) is a critical activity within clinical trial monitoring, yet the traditional approach focused on 100% SDV is limited in its ability to quickly identify issues and prevent them from recurring. Rave TSDV (Targeted SDV), unified with Rave EDC, enables CRAs to focus on critical to quality (CtQ) factors identified within risk management activities.
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Feasibility As A Service From Consulting & Analytics
11/26/2024
Citeline’s Feasibility as a Service (FaaS) leverages data-driven insights to enhance clinical trial success by providing comprehensive feasibility assessments.
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Delivering High-Quality Patient Outcomes Data
9/16/2025
Delivering high-quality patient outcomes data with patented technology, rapid deployment, and expert guidance.
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The Next-Generation Of Clinical Trial Data Management And Operations
6/19/2025
This platform benefits sponsors seeking faster study cycles and regulatory compliance, CROs, MedTech companies, and research sites globally.