Inductive EDC
Streamline your clinical research with AI-led automation
Use Inductive EDC and its powerful features to transform your clinical research data management and accelerate your way to approvals.
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.
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.
Create your study setup with pick-and-choose modules to design CRFs that require zero learning curve
Invite, add and manage multiple users with various permission controls accessible from a single hub
Ensure global compliance like FDA CFR Part 11, ICH GCP (HIPAA), GDPR (EU), ISO 27001, and ISO 9001.
Start small and scale as your study progresses without the worry of overloading the platform
Use either API or direct data upload with a one-click process to import data from external sources
Allow mid-study changes by easily editing forms without the need for rescuing from tech support
Intelligent query management allows you to access data in real-time, which also facilitates faster analysis
Build easily understandable reports with attractive visuals like bar charts, line graphs, and scattering plots
Set event-based or time-based schedules to trigger alerts and send notifications to concerned stakeholders