Emergo by UL has rolled out an enhanced version of its Regulatory Affairs Management Suite (RAMS) platform to provide automated, efficient and cost-effective regulatory affairs and quality management support for medical device companies.
RAMS 2.0 features an expanded set of digital tools and capabilities to enable medical device as well as combination product manufacturers to more effectively manage and monitor registration and compliance activities across more than 20 markets worldwide.
Key features of RAMS 2.0 include weekly insights and regulatory intelligence updates from Emergo by UL consultants, interactive planning tools for FDA 510(k) applicants, and searchable databases of regulatory documents and resources covering all markets in which Emergo by UL is active.
Until December 31, 2020, manufacturers may sign up for RAMS 2.0 accounts at no charge to discover the benefits of digital RA/QA management.
Manufacturers may learn more about our RAMS 2.0 launch in our press release.
Exhibitor Data Sheet