RESEARCH & THOUGHTS
Perspectives Shaping Clinical Development
Discover engaging resources driving the conversation forward and on-demand demo videos showcasing the very solutions forming the future of our field.
CluePoints’ Site Profile & Oversight Tool (SPOT) enables adaptive site monitoring so teams can swiftly...
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Site monitoring is one of the most expensive components of clinical trials; on-site monitoring alone...
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In clinical trials, patient data such as adverse events and concomitant medications is coded against...
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Swiftly pinpoint anomalies and translate insights into actionable strategies with adaptive site monitoring.
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Explore clinical and operational data from various perspectives and domains in configurable formats with...
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Test all collected data, including both clinical and operational, exposing atypical patterns that indicate...
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Empower Clinical Trial Teams with ML
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The Risk-Based Data Management Revolution
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Your RBQM Benchmark Analysis: Prepare for ICH E6 R3
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CluePoints Intelligent Analytics Platform
- Research Paper
Does Central Statistical Monitoring Improve Data Quality? An Analysis of 1,111 Sites in 159 Clinical Trials
- Research Paper
Tufts Center for the Study of Drug Development Impact Report: Analysis & Insight Into Critical Drug Development Issues
- Research Paper
The Eradication of False Signals in Monitoring
- Research Paper
Statistical Monitoring of Data Quality and Consistency in the Stomach Cancer Adjuvant Multi-Institutional Trial Group Trial
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Data-Driven Risk Identification in Phase III Clinical Trials Using Central Statistical Monitoring
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The Role of Biostatistics in the Prevention, Detection, and Treatment of Fraud in Clinical Trials
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A Statistical Approach to Central Monitoring of Data Quality in Clinical Trials
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Centralized Statistical Monitoring as a Way to Improve the Quality of Clinical Data
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ICH E6 R2 – The Clinical R&D Industry’s Response
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Beyond Risk-Based Monitoring: How Intelligent Analytics Are Being Used To Drive Value And Support ICH Compliance
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The Bigger Picture Of ICH E6 R2: Looking Beyond Compliance
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ICH E6 R2: Talking Big Pharma’s Response To The Addendum
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ICH E6 R2 Roundtable Review – What Does This Mean For The Industry?
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ICH E6 R2: Waiting And Watching No Longer An Option When It Comes To Risk-Based Monitoring
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ICH E6 (R2) – Miracle Pill For The Clinical R&D Industry
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ICH E6 Rev 2 – Ask The Experts
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Webinar Recording: What Does ICH E6 R2 Mean For Me And My Company?
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6th Annual CROWN Congress: Sessions You Can’t Afford To Miss + 15% Discount Code
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Six Ways To Get The Most Out Of Outsourcing In Clinical Trials West Coast ‘17
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The FDA Is Knocking At Your Door – Are You Ready For An FDA Site Inspection?
