Randomization eliminates biases by randomly assigning participants in clinical trials to different groups (such as treatment or control groups). This is done so that every participant has an equal opportunity to be allocated into any of the groups, reducing confounding factors both known and unknown, including age, gender, and baseline health status. Randomization also increases the reliability of the trial results by eliminating the possibility that researchers or participants could influence group assignment.
Our Randomization Services
- Web-based & automated randomization solutions
- Reduces site-level bias
- Ensures real-time allocation control
- Balances treatment groups based on critical factors (e.g., age, gender, disease severity)
- Maintains trial integrity and improves data accuracy
- Controls balance across treatment groups
- Ideal for multi-site clinical trials
- Dynamic assignment based on real-time trial data
- Increases efficiency and ethical balance
Seamless IRT system for patient randomization and drug supply management
Real-time tracking and reporting
Why Choose Us?
Regulatory Compliance: FDA, EMA, and ICH-GCP compliant solutions
Real-time Monitoring: Live tracking and reporting for sponsors and CROs
Customized Solutions: Tailored randomization based on trial needs
Secure & Reliable: Data encryption and audit trails