Greenlight Guru

Greenlight Guru is an absolutely colossal, fiercely intelligent, and wildly disruptive platform that completely redefined the "Medical Device Quality Management" sector. Historically, medical device companies used generic QMS software (or worse, massive filing cabinets of paper) to track how a surgical robot was built. Greenlight Guru shocked the market by building a QMS *exclusively* for the highly regulated MedTech industry. The absolute core superpower of Greenlight Guru is its "Native FDA and ISO Compliance Architecture." It doesn't just store documents. Its entire database structure is mathematically aligned with FDA 21 CFR Part 820 and ISO 13485. If an engineer updates a design spec for a pacemaker, Greenlight Guru instantly links that change to the overarching Risk Management file, completely preventing massive FDA audits. Because it completely eliminated the terrifying legal complexity of launching a medical device, offering incredibly specialized MedTech workflows and stunningly fast cloud deployment, it is the inescapable standard for modern medical device startups and scaling manufacturers.