Navigate RA/QA activities with powerful tools that simplify your work and provide market insights.
Streamline the first step to market access with device classification and verification.
Build documentation faster and reduce errors using guided step-by-step tools.
Simplify your work with automated registration and certification tracking.
Track regulatory changes across multiple markets that impact your device registrations.
Access detailed regulatory roadmaps by country, device type, and device class.
Get new devices to market faster through the eQMS provided by Greenlight Guru.
Easily prepare and maintain Clinical Evaluation Plans and Clinical Evaluation Reports that comply with the MDR and MDCG guidance.
Simplify your work with automated registration tracking, certification tracking