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.
Your eCRFs speak volumes.
Want better data, faster? Focus on your forms.
Get it right the first time, every time.
Sophisticated (but easy-to-set) edit checks help ensure cleaner data from the start.
Get your forms talking.
Cross-form intelligence means eCRFs that are responsive to any element of your dataset,
from the participant’s last recorded blood pressure to the expected date of a missing form.
Auto-save the day.
Become a hero for your sites with auto-save on every field change.
Brains AND beauty.
Discover a clean, mobile-friendly UI that actually engages sites and participants.
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.
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.
Crystal clear forms and real-time validation checks ensure cleaner data from the start.
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.
“OC4 is extremely user friendly for both administrators and users. The study build is straight forward, allowing for powerful eCRFs to be designed, developed and validated with ease. Excellent customer support.”
David Murray | Senior Trials Programmer
“OpenClinica makes it easy for us to quickly deploy an intuitive and highly capable data capture experience to support our sponsors’ demanding needs for high quality clinical data.”
James Liu | QA Director
“OpenClinica gives us the freedom to conduct as many trials as we want to and the flexibility to do things our way. Working with OpenClinica always makes me feel like my concerns are heard and taken seriously, even though we are a small company.”
Liz Robertson | Sr. Director, Bioinformatics