Without an EDC system, the travel time for study data between computers, data managers, and supervisors increase further delaying the conclusion of your clinical research.
Inductive EDC removes all the roadblocks to achieving a seamless data management environment that expedites your study, improves data quality, and complies with regulatory standards. Our EDC system allows you to configure the CRFs for any specific need including academic, biotech, and pharmaceutical study. It ensures greater data privacy and security, along with inherent compliance.
Our EDC platform is a cost-effective option to help you collect, analyse and manage data in mammoth quantity reducing your dependency on the paper-based process.
Inductive EDC Features
Manage your clinical trial data with full confidence with Inductive EDC which empowers you with smart and user-friendly features to ensure you are in charge of your entire study.
Set event-based or time-based schedules to trigger alerts and send notifications to concerned stakeholders
Manage your clinical study from one platform
Create a personal, central clinical data management hub
Operate the entire clinical study from one single place
Centralize your clinical study operations by bringing all the data sets onto a single platform for a comprehensive analysis, greater control and faster conclusion