Unrivaled data visibility and management
Run faster, smoother studies with real-time insight into study
progress and data and workflows that comply with FDA, EU
MDR, and ISO 14155:2020 requirements.

Quickly build eCRFs using pre-validated question types
Easily collect clinical data with modern electronic case report forms (eCRF).
Build forms in minutes with Greenlight Guru’s eCRF software, then clone, reuse,
and improve them to streamline study design and execution.

Get higher response rates with patient-friendly ePRO
Collect high-quality patient-reported data with ePRO software
that allows patients to simply and securely fill out forms from their
phone without downloading an app.

Fast and friendly informed consent
Simplify informed consent with eConsent that’s compliant
with Part 11 and EU standards for electronic signatures.

Add randomization to any study
Handle RTSM (Randomization and Trial Supply Management) in
the same system you use for everything else, with support for
both block and stratified randomization.

Collect post-market data from any source
Meet all your post-market data requirements with support for PMCF
studies, PMCF survey software, and registry ready templates that simplify data collection.

Stay compliant with built-in AE reporting
Ensure timely and compliant adverse event reporting with dedicated AE/SAE
reporting software that meets the requirements of ISO 14155:2020.

Easy and secure data transfers
Push and pull data from your studies with Greenlight Guru
Clinical’s two-way API. Integrate with third-party apps for fast and
secure data flow across platforms.