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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- Research Paper
Linear Mixed-Effects Models for Central Statistical Monitoring of Multicenter Clinical Trials
- Research Paper
Linear Mixed-Effects Models for Central Statistical Monitoring of Multicenter Clinical Trials
- Research Paper
Use of the Beta-Binomial Model for Central Statistical Monitoring of Multicenter Clinical Trials
- Research Paper
Ensuring Trial Validity by Data Quality Assurance and Diversification of Monitoring Methods
- 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
- Whitepaper
Examining the Current State of ICH E6 (R2) Adoption
- Whitepaper
From RBM to RBQM: The Future of Risk-Based Trial Management
- Whitepaper
Harnessing CSM to Drive Risk-Based Quality Management (RBQM)
- Whitepaper
Conclusions from Executive Roundtable on Response to ICH E6 (R2)
- Whitepaper
Implementing a Scalable Risk-Based Monitoring Strategy
- Whitepaper
Sponsor Responses to the ICH E6 Revisions
- 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
- Blog
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?
