Randomization
Randomization eliminates biases by randomly assigning participants in clinical trials to different groups (such as treatment or control groups).
Supplies
Clinical trial supplies include everything needed to run a study, including equipment and resources. This also includes investigational medicinal products (IMPs), ancillary supplies.
Returns
Returns in clinical trials are the cyclic return of unused, expired, or damaged clinical trial supplies from study sites. Proper management of returns ensures compliance with regulatory guidelines and helps maintain study integrity.
Integration
Integrations in clinical trials refer to the process of connecting multiple digital systems and platforms to facilitate operations, increase data transfer, and increase efficiency in general.
EDRS
EDRS, or Electronic Data Record System, is a tool used for managing clinical trial information. It is the central system used for collecting, storing, and organizing data as it comes in, like a paper-based system
ePRO
ePRO solutions adhere to global regulatory standards, including FDA, EMA, HIPAA, and GDPR. This ensures that patient data is handled securely, with strict compliance to safeguard privacy and maintain the integrity of clinical trials.
eCOA
eCOA enhances patient engagement, reduces paper-based assessments, and supports remote patient monitoring, enabling faster and more accurate clinical trial results.
UAT Services
UAT Services ensure that a system meets business requirements and user expectations before deployment. It involves real-world testing by end-users to validate functionality, usability, and performance.