CDISC and OpenClinica Collaborate to Drive Academic Clinical Research Forward
CDISC will instantiate electronic Case Report Forms (eCRFs) from its eCRF Portal into OpenClinica’s Electronic Data Capture (EDC) content library so that academic researchers can leverage the eCRFs to easily adopt CDISC Standards while capturing data for their studies. Implementing CDISC standards allows data to be structured effectively, leaving academics more time to focus on discoveries that will have invaluable impact on clinical research.
Clinical Data Management: Using the most versatile eCRFs available.
A fully compliant, all-in-one platform for every type of study.
Electronic Data Capture &
Clinical Data Management
Create beautiful, ultra-capable eCRFs, featuring
real-time edit checks, skip logic, and auto-save.
Design studies on a simple, drag-and-drop interface.
Randomization &
Supply Management
Add randomization to your studies, with all common randomization methods.
Track drug kits and monitor inventory in a seamless, integrated user experience.
Patient reported outcomes
(ePRO and eCOA)
Collect cleaner data, faster, with user-friendly forms.
Engage study participants on their own devices
no matter their location.
Reports Built With You In Mind
Operational and clinical data visualized with bar charts, line graphs, and more.
Automate the distribution of reports to act quickly to major world events or every day queries.
Complete validation documentation and audit support.
Reduce Queries
Crystal clear forms and real-time validation checks ensure cleaner data from the start.
Lock Faster
Keep everyone on schedule with actionable reporting for study leaders, monitors, and sites.
