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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- Infographic
Your Journey to Adaptive Site Monitoring
- Blog
Meet SPOT: Transforming Site Monitoring Practices with Adaptive Intelligence
- Blog
A New Era of Automation: Improving Efficiency & Outcomes with Intelligent Medical Coding
- Demo Video
Site Profile & Oversight Tool (SPOT)
- Swiftly pinpoint anomalies and translate insights into actionable strategies with adaptive site monitoring.
- Demo Video
Business Intelligence (BI)
- Explore clinical and operational data from various perspectives and domains in configurable formats with multiple data widgets.
- Demo Video
Central Statistical Monitoring
- Test all collected data, including both clinical and operational, exposing atypical patterns that indicate challenges.
- Demo Video
Duplicate Patients
- Specify configurable variables likely to indicate duplicates and review based on similarity scores and side-by-side evaluations.
- Demo Video
Key Risk Indicators (KRIs)
- Rank sites based on performance and tolerance metrics, uncovering ‘at-risk’ locations in need of corrective action.
- Demo Video
Patient Profiles
- Flag atypical patient patterns, prioritize investigations into anomalies within data sets, and determine critical targets.
- Demo Video
Quality Tolerance Limits (QTLs)
- Identify systematic issues, monitor key metrics, and document deviations from pre-defined QTLs to ensure compliance.
- Demo Video
Risk Assessment & Mitigation
- Determine vulnerable trial areas, define risk controls, and monitor capabilities to detect evolving threat levels.
- Demo Video
Signals & Actions Tracker
- Assess identified issues, annotate commentary, deploy automatic auditing, and leverage extensive exporting capabilities.
- 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
- 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?
