A complete one-stop solution to collect and manage all clinical trial information across all phases, therapeutic areas, magnitude or complexity of the studies.
An easy to use and cost-effective integrated solution that delivers data solutions on-demand for pharmaceutical, biotechnology, medical device companies, Contract Research Organizations and Data Management companies.
vData-eDC
vClin-ctms
Dispense-iWRS
vSafety-PV
vFile-eTMF
vPro-Diary
vQuality-qms
vSource-rSDV
vData-eDC™ is ideal for all clinical trials regardless of phase, therapeutic areas, magnitude or complexity.
vClin-ctms™ is a web enabled clinical trial management system that supports to view and manage real-time operational performance.
vDispense-iwrs™ is a web enabled interactive web response system for managing study randomization and supply management solutions.
vSafety-PV™ is compliant to EMA and FDA regulatory requirements and is aligned to ICH ICSR (R2).
vFile-eTMF™ covers full document life cycle from document creation to document review, approval and validation.
vPro-Diary™ is a web-based system that helps for instant data capture from patients and transfer to a centralized data center from anywhere in the world.
Writing audit reports and performing CAPA has never looked so easy with our Audit Reports and CAPA Management solution.
The coronavirus disease 2019 (COVID-19) pandemic has rapidly challenged the pharmaceutical industry to implement remote clinical trials.
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