Collect high-quality, compliant data from clinicians, patients, and any other users—and manage it all in the same system. Built specifically for MedTech, Greenlight Guru is the only clinical data solution you’ll need, from premarket studies to post-market surveillance and PMCF activities.
Whether you're preparing for a pilot study or sending out post-market surveys, Greenlight Guru makes it easy to collect and manage all your clinical data in a modern, compliant, and user-friendly system. Say goodbye to paper and hello to intuitive design and unrivaled visibility into your data.
With a full suite of eCRF, ePRO, post-market surveys, and ad hoc data collection methods, you never miss out on crucial clinical data.
Mobile-friendly and modern collection options mean higher response rates, better adherence, and excellent data quality.
Greenlight Guru’s EDC system comes pre-validated per FDA, EU, and ISO 14155:2020 requirements, so you can begin your clinical activities in compliance and stay that way.
Ready-to-use and customizable compliance templates, combined with in-house industry experts, mean you’re never on your own.
Our no-code solution ensures that anyone can quickly learn how to use Greenlight Guru, create studies, and navigate the system with ease.
Build studies in as little as 90 seconds, reuse forms and studies to save time, and get real-time insight into your data.
An EDC for medical device, IVD, and SaMD clinical trials.
MedTech studies are different. That’s why you won’t find expensive, pharma-centric features in Greenlight Guru’s EDC system.
You’ll have everything you need to collect and manage high-quality clinical data—and nothing you don’t.