Navigate RA/QA activities with powerful tools that simplify your work and provide market insights.
Simple solutions that target your medical device or IVD expansion.
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.
Plan your expansion with process charts and FAQs comprising a global knowledge base.
Discover Greenlight Guru's eQMS platform and learning management from ComplianceWire®.
Access detailed regulatory roadmaps by country, device type, and device class.
Manage your transition from MDD to MDR and prepare for IVDR implementation with a wide range of dedicated Smart Builders.
Simplify your work with automated registration tracking, certification tracking