Greenlight Guru Alternative for Medical Devices

While Greenlight Guru provides design control workflows for early-stage medical device R&D, growing MedTech companies quickly encounter severe operational boundaries once products enter commercial production.

First, Greenlight Guru lacks native manufacturing execution (MES/eDHR). Medical device plants are forced to maintain paper traveler binders or purchase disconnected third-party software to record serialized assembly, component lot reconciliation, and shop-floor line clearance.

Second, Greenlight Guru charges steep per-seat fees ($200 to $350 per user per month), making it economically impossible to provide digital accounts to assembly technicians, cleanroom operators, and incoming QC inspectors. Novaqis eliminates this seat tax with flat facility licensing, delivering a unified platform that connects DHF design controls, eDHR manufacturing execution, ISO 14971 risk management, and QC laboratory testing on a single database fabric.