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.
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.
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.
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.
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.