Services
Tailored services that get your global trials out into the world on time and on budget
Insight-Driven Planning
The way a clinical trial is set up is vital to its success. We partner with clients early to identify objectives, high value tasks, risk indicators, potential biases and critical study endpoints. Our monitoring plans ensure studies are safe, compliant and efficient across their lifespan.
Protocol Development
Statistical Considerations
Efficient Trial Design
Sample Size Calculations
Monitoring
Plans
Randomization Plans
Risk Assessment Planning
Monitoring
Plans
Randomization Plans
Risk Assessment Planning
Rapid Setup
Need a team of experts to set up your trial for maximum efficiency, speed and usability? Let us set up your database, CRFs, edit checks, code lists and procedures so that you get more accurate outcomes in less time. We can also verify your existing end-to-end setup and make improvements that will shave months off trials.
CRF design and consulting
Database setup, testing and validation
Edit check development
Built-in data analytics
Seamless Study Conduct + Operations
WHO and MedDRA Coding for Standardization
Database Design, Data Monitoring and Verification
Integrated Randomization Implementation
Customized Dashboards for Progress Monitoring
eConsent Interactive Platform
ePRO Mobile App Setup
Automated Reports For Tracking
eConsent Interactive Platform
ePRO Mobile App Setup
Automated Reports For Tracking
Advanced Data Analytics
Our cross-disciplinary team combines clinical trial development expertise and programming know-how to make sure your data collection synergizes with data analysis downstream. We offer comprehensive statistical analysis, including TLFs, and interim statistical analysis for adaptive designs.
Integrated Analytics
Statistical Analysis Plans (SAP)
Statistical Analysis and Programming
Comprehensive Reporting
