By delivering high-quality clinical data that has been pre-cleaned, our e-clinical systems make your study significantly more productive.
Configure studies quickly with our simple and inbuilt interface without depending on programming.
Form rules like edit checks and conditional branching along with user friendly data entry forms empower users to enter data rapidly while ensuring accuracy.
Clinion a complete and integrated environment for the configuration,
data capture and data management of clinical trials.
Clinion global library is now integrated with SDTM libraries so that SDTM annotations can be mapped to CRF fields during eCRF creation. Features of SDTM integration include:
Quick and Faster
Doesn’t depend on programmers
or other contractors
Ensure precision with real-time
edit checks, skip logic, and other highlights
Adequate monitoring with
Integrated with IWRS, CTMS, RBM and CDISC solutions
Workable from multiple
devices and browsers
Simple and easy to
Clinion is ideally suited for Phase II – Phase IV interventional and observational studies. Clinion has been deployed for FDA, EU, Israel & Indian regulatory studies. The major therapeutic areas covered by Clinion are: