Fewer fires.

Faster studies.

Lean teams can’t afford delays. OpenClinica gives CROs the real-time oversight, compliance, and speed sponsors expect—without adding tools.

Who It’s For

Academic medical‑center researchers collaborating in a lab or hospital setting on clinical studies.

CROs running clinical trials, disease registries, post-marketing studies, and real-world evidence programs

Investigator manages multiple independent studies (5–100 active trials per year) using streamlined eClinical tools.

Ops teams managing multiple studies across sponsors

Research team transitions from spreadsheets and DIY tools to a unified clinical‑trial platform for improved efficiency.

Lean teams that need sponsor-grade performance fast

Benefits

Launch fast

Start studies in days, not months

One workspace

Oversight, EDC, and randomization in one place

Sponsor-ready

Compliance and audit trails included

More value, fewer vendors

Consolidate your stack and win more bid

Predictable pricing

Flat-rate packages that scale with your portfolio

Accelerated enrollment

Use Recruit to support site adoption and patient outreach

Used by CROs supporting over 50 concurrent studies

How it Works

  1. Build & Configure

    Set up CRFs and workflows fast with intuitive tools

  2. Activate Oversight

    Enable dashboards and query alerts to track milestones

  3. Capture & Randomize

    Use built-in eConsent, eCOA, and Randomization

  4. Deliver Results

    Provide live dashboards to your sponsors

Ready to deliver sponsor-grade results without the bloat?

Pricing & Packages

Recommended Products

Ready to get started?

Tell us about your needs. Our team will help you find the right solution and answer any questions about how OpenClinica can support your work.

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