Greenlight Guru for CROs

Collect and manage high-quality clinical data with a modern, easy-to-use EDC system built specifically for MedTech. With Greenlight Guru, you get a powerful, compliant, and easy-to-use system that makes study setup and monitoring a breeze.

Ditch the clunky, pharma-centric systems

Greenlight Guru Clinical is the only solution you'll ever need for medical device clinical trials. When you partner with Greenlight Guru, you get built-in compliance to US and EU regulations, a modern and user-friendly UX, and the highest-rated customer success team in the industry.

1,100+ of the world’s leading MedTech companies trust Greenlight Guru.

Why CROs Love Greenlight Guru

Pre-validated for MedTech

Our software comes pre-validated per FDA, EU MDR, and ISO 14155:2020, so you can be sure your data collection and management is compliant without any complex customizations.

Automatic audit logs, permission-based access, and two-factor authentication mean that your data is always secure and traceable.

No coding necessary

Our no-code EDC system allows your team to get up and running quickly—whether they have technical expertise or not.

A three-step study builder and a modern, intuitive interface streamline study builds with flexible and scalable elements that can handle studies of any size or complexity.

Unrivaled data visibility

When you choose Greenlight Guru, you get extensive data management and reporting capabilities that ensure you always have a real-time overview of study progress and clinical data.

Get immediate insight into different study sites, build and customize reports, and react immediately to issues or changes in your studies.

Choose how you partner

With multiple ways to partner, you can choose how best to deploy Greenlight Guru for your MedTech clients.

You’ll also become part of our worldwide partner network, the premier destination for MedTech companies looking for services and solutions to help drive their success.

Built for Customers Like You

“Our partnership with Greenlight Guru has meaningfully influenced our success by directly impacting operations efficiency and adherence to timelines.”

Lucie Pribylova

Commercial Operations, HEMEX

“Data monitoring is much easier now than it was before. It's much easier to follow the participant flow and see the status of each participant. Before, we had to write to the site and ask for that status.”

Sarah Nygaard Jensen

Clinical Project Manager, InnoCon Medical

“Having everything-informed consent, randomization, and the eCRFs and ePROs- all in one system makes it much easier to finish the study on time. The teams at our study sites also really value that they don't have to work with more than one system.”

Heiða Bragadóttir

Clinical Trial Manager, Sidekick Health

“The requirements for medical devices are very different from the requirements of pharmaceutical trials, so we needed and EDC solution specifically for medical devices.”

Martijn Dekkers

Clinical Research Manager, Medartis