Less patchwork.

More progress.

Too many disconnected tools? OpenClinica gives academic teams a single platform to launch compliant studies faster, with less stress and more control.

Who It’s For

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

Academic medical centers and research institutes

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

Investigator-initiated studies with 5–100 active trials per year

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

Teams outgrowing DIY tools and spreadsheets

Benefits

Faster study start-up

Go live in weeks, not months

IRB-ready from day one

Built-in Part 11 compliance and audit trails

Unified workflows

eConsent, EDC, and reporting all in one place

More research, less admin

Spend time on science, not systems

Transparent pricing

Packages aligned to grant budgets

Trusted by 100+ research institutions and academic medical centers

How it Works

  1. Design & Launch

    Drag-and-drop builder + compliant templates = studies built without IT

  2. Consent & Capture

    Multimedia eConsent and mobile-friendly eCOA feed clean data into your EDC

  3. Monitor & Report

    Dashboards track enrollment, queries, and compliance in real time

  4. Export & Analyze

    Easily export de-identified datasets for analysis, publication, and grant reporting

  5. Share & Reproduce

    Support transparency, reproducibility, and FAIR data practices with integration pathways like FHIR, OMOP, and HL7

Ready to make research smoother?

Pricing & Packages

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