What we do
Our expertise lies in developing dedicated software to elevate your research endeavors, enabling streamlined data collection, efficient document management, precise drug administration, adverse event tracking, and logistics management tailored for the clinical research world.
Electronic Case Report Forms (eCRF)
Effortlessly capture and manage critical subject data through our advanced Electronic Case Report Forms. Designed for seamless integration and user-friendliness, our eCRF solution empowers researchers to collect, oversight, and analyze clinical data with utmost precision and efficiency.
Electronic Trial Master File (eTMF)
Stay organized and compliant with our Electronic Trial Master File solution. . Securely manage all essential trial documents, from eTMF to Investigator’s Site File documents, ensuring seamless collaboration and a complete overview of your clinical trials.
Electronic Clinical Drug Supply (eCDS)
Optimize Investigational Medicinal Product (IMP) management with our eCDS system. From inventory tracking to precise IMP accountability, our solution ensures accurate IMP oversight and minimizing wastage.
Safety Database
Track and analyze serious adverse events effortlessly with our dedicated Safety Database. Designed to meet rigorous regulatory standards, our solution empowers safety monitoring, risk assessment, and reporting, safeguarding the well-being of trial participants.
Clinical Logistics Management
Efficiently manage the logistics of clinical research, including the transportation of biological samples, with our specialized solutions. Our comprehensive logistics management system ensures traceability of biological samples, timely and secure delivery, enabling effective collaboration between stakeholders.
Integration Services
Our expert team provides continuous integration of all our software systems, offering a unified and efficient platform to manage clinical trials, streamline processes, and enhance collaboration among stakeholders.