Any time.

Any where.

Any device.

Fun and frictionless patient reported outcomes. 

ePRO and clinical data, together as one.

Patient-reported data instantly part of your overall study data set.

Get data that’s fresh in your patient’s mind.

Automated SMS and email reminders.

Patient centric convenience.

Your trial subjects use their own device. No app. No password.

GCPeace of mind.

ePRO data that’s HIPAA compliant and fully auditable.

Transparency at last.

Instantly monitor and track your ePRO form statuses.

OpenClinica Participate automatically unifies data we collect directly from our patients with our other study data. We only have to build forms once.
Abigail Allen

Director, Clinical, MCRA - Musculoskeletal Clinical Regulatory Advisers

Download our white paper, “Captured in the Wild.”

In ten minutes, learn from three recent examples of real-world data collection that ensured quality while driving down costs.

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