We have a Cloud-based easy to use, regulatory Compliant, end-to-end Electronic Data Capture (EDC) / eCRF system. Which manage all clinical data management aspects including Study Planning, Study build, Study Conduct, Discrepancy / Queries management, Medical Coding, Data Extract Our System is integrated to manage CAPA, Change, Deviations, Audits, Compliance documents, Training, etc of a Clinical Trial. Our system ships with inbuilt Metadata and Master Data Management modules to manage Study Global Libraries, Sites, Investigators, Products, and other master data in a centralized repository and provides a higher level of reusability of the information in different clinical trials.