Better data, faster, in two days. 

Attend OC18 on October 15 and 16 in Boston.

Clinical data management this powerful has never been this easy.

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Clinical data management
this powerful
has never been
this easy.

Request a demo

Get better data, faster, with 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

Easily design studies on a drag-and-drop interface

Create beautiful, ultra-capable eCRFs featuring
real-time edit checks, skip logic, and auto-save

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Patient reported outcomes
(ePRO and eCOA)

Engage study participants on their own devices

Collect cleaner data, faster, with user-friendly forms

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Randomization &
Supply Management

Easily add randomization to your studies

Seamless, integrated user experience

Supports all common randomization methods

Track drug kits and monitory inventory

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Reporting

Operational and clinical data, for acting quickly on everything from queries to adverse events

Visualize with bar charts, line graphs, and more

Automate distribution of reports

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4,000+ studies. 5M+ participants.

REDUCE QUERIES

Crystal clear forms and real-time edit 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.

“Switching over from paper to EDC started out as an overwhelming task. After going through countless sales processes and demos, OpenClinica was a breath of fresh air. OpenClinica is a robust program with incredible flexibility, and extremely cost effective.”

Laura Richie | Director of Data Management

“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

“Switching over from paper to EDC started out as an overwhelming task. After going through countless sales processes and demos, OpenClinica was a breath of fresh air. OpenClinica is a robust program with incredible flexibility, and extremely cost effective.”

Laura Richie | Director of Data Management | Cancer Insight

“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 | FMD K&L

“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 | Tracon Pharma

Read more user experiences on Capterra.

Request a demo