Emergo by UL’s Regulatory Affairs Management Suite (RAMS) provides automated regulatory compliance management capabilities for medical device manufacturers across markets worldwide.
More than 1,700 companies rely on RAMS to make sure their device registrations and certifications remain valid. They can also access digital tools for device classification, prepare submissions to the U.S. Food and Drug Administration and other regulators, and find actionable medical device regulatory and market intelligence.
Affiliate software services for quality and learning management are also available via RAMS.