Clinical Technologies Solutions
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Full Visibility For Study Teams And Control Over Consent
9/16/2025
Enhancing patient comprehension and giving study teams full visibility and control over consent throughout your trial.
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Don't Let Staffing Shortages Slow Down Your Clinical Trial Conduct
10/13/2022
Prevent trial delays by empowering your CRAs to monitor more sites per week, focus on strategic activities, and work with a wide range of sites, enabling remote monitoring and document sharing.
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IQVIA Safety Notifications
5/20/2020
Now featuring cross-trial functionality, IQVIA Safety Notifications gives sponsors and contract research organizations (CROs) a centralized, simple solution for disseminating, managing, and tracking SUSARs and other safety notifications.
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Suvoda RTSM (IRT)
9/16/2025
A centralized command center for patient randomization and drug supply management—built for today’s complex clinical trials.
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Wearable Device Comparison Guide: Medical-Grade Or Consumer Device?
5/15/2024
Explore the specifications of different types of wearable devices to find the optimal solution for your study, and consider how integration can elevate your clinical development program to new heights.
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TrialKit eSource (Direct Data Capture)
6/6/2024
Gain confidence in your clinical research data with direct data capture (DDC).
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What Does 'Powered By Block Clinical' Mean?
12/8/2025
Join us in supporting every part of the clinical trial ecosystem — patients, caregivers, sites, and suppliers — to ensure trials run safely, efficiently, and successfully.
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Get Your Tile Into One Home
7/15/2024
For clinical trial technology vendors, it’s fast and easy to become part of the only industry-wide solution to sit tech overload.
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Who We Work With And What We Do For You
7/20/2026
TruTechnologies: Clinical Trial Execution, Live
TruTechnologies (Tru) is the industry’s first clinical trial execution system, delivering truly real-time visibility into trial execution at the point of care.
And it’s about time.
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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.