Founded in 2006 by medical device engineers frustrated with the inefficiencies and risks of paper-based systems, Greenlight Guru set out to build a modern, purpose-built solution for MedTech quality and clinical processes. Today, it supports over 1,100 customers globally with tools spanning document control, design control, risk and CAPA management, audit preparation, supplier management, and more designed to ensure audit readiness and traceability across the device lifecycle. Greenlight Guru blends intuitive, MedTech-specific workflows with a rich educational ecosystem including its Academy, blog, podcasts, and templates positioning itself as not just a software provider but a growth partner for device companies aiming for quality, speed, and compliance.