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.
In a world where complacency is the enemy of progress, Contract Research Organizations (CROs) stand at...
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- Guide
Empower Clinical Trial Teams with ML
- Guide
The Risk-Based Data Management Revolution
- Guide
Your RBQM Benchmark Analysis: Prepare for ICH E6 R3
- Guide
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
- Research Paper
Data-Driven Risk Identification in Phase III Clinical Trials Using Central Statistical Monitoring
- Research Paper
The Role of Biostatistics in the Prevention, Detection, and Treatment of Fraud in Clinical Trials
- Research Paper
A Statistical Approach to Central Monitoring of Data Quality in Clinical Trials
- Research Paper
Centralized Statistical Monitoring as a Way to Improve the Quality of Clinical Data
- Research Paper
Impact of On-Site Initiation Visits on Patient Recruitment and Data Quality in a Randomized Trial of Adjuvant Chemotherapy for Breast Cancer
- Research Paper
Data Fraud in Clinical Trials
- Research Paper
Does Central Monitoring Lead to Higher Quality? An Analysis of Key Risk Indicator Outcomes
- Research Paper
Detection of Fraud in a Clinical Trial Using Unsupervised Statistical Monitoring
- Blog
ICH E6 R2 – The Clinical R&D Industry’s Response
- Blog
Beyond Risk-Based Monitoring: How Intelligent Analytics Are Being Used To Drive Value And Support ICH Compliance
- Blog
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
- Blog
ICH E6 R2 Roundtable Review – What Does This Mean For The Industry?
- Blog
ICH E6 R2: Waiting And Watching No Longer An Option When It Comes To Risk-Based Monitoring
- Blog
ICH E6 (R2) – Miracle Pill For The Clinical R&D Industry
- Blog
ICH E6 Rev 2 – Ask The Experts
- Blog
Webinar Recording: What Does ICH E6 R2 Mean For Me And My Company?
- Blog
6th Annual CROWN Congress: Sessions You Can’t Afford To Miss + 15% Discount Code
- Blog
Six Ways To Get The Most Out Of Outsourcing In Clinical Trials West Coast ‘17
- Blog
The FDA Is Knocking At Your Door – Are You Ready For An FDA Site Inspection?
