Built for Every Stakeholder

From CROs and sponsors to sites and academics, Clinavare
connects the entire clinical trial ecosystem on one platform

For Research Sites

All your essentials in one place eReg binders, logs, and document control, to keep your site organized and audit-ready.

For CROs

Streamline oversight with standardized workflows, centralized documentation, and real-time visibility across studies and sites.

For Sponsors

Gain confidence with real-time compliance reporting, transparent document access, and audit-ready records at every stage.

For Academic Trials

Simplify trial management with secure digital tools that reduces administrative burden and supports compliance for NIH, DOD, and NSF-funded studies.

Compliance at the Core

With Clinavare, compliance isn't an add-on, it's built into every feature.
Security, oversight, and audit readiness are integrated from day one to protect your data at every step.