Six Must Know EDC Guidelines
How can you make sure that the study protocol is implemented in a way that maximizes efficiency and data quality? Getting the details right during the build phase paves the way for a smoother study, generates better data, and keeps stakeholders productive and positive.
Do you follow all six?
Clinical Data Management: Better data, faster, from 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.
Save Over Paper
Ditch the diaries and purge the paper CRFs. Deliver a secure, mobile-friendly experience on any device.
