Utilizing RAMS for efficient medical device RA/QA management

Medical device and IVD manufacturers who use or are considering using the Regulatory Affairs Management Suite (RAMS) digital platform will benefit from this summary of its current features as well as new and upcoming enhancements. The RAMS SaaS (software as a service) offering provides an array of tools allowing companies to track device registrations and stay up to date with regulatory changes.

Foremost among the recent additions in RAMS is 510(k) Builder, a subscription service that helps manufacturers create submissions for FDA premarket clearance. In this webinar, presenters Anil Vasireddy and Kristi Gusman will demonstrate how 510(k) Builder works, along with new updates that refine the existing RAMS functionality.

If you are unclear on what your company could be getting out of RAMS, this webinar is the perfect opportunity to gain understanding of the full range of free and premium services available on this platform.



Anil Vasireddy | Director, Product Development

Kristi Gusman, PMP | Product Owner

Elizabeth Manning,  | Program Manager, Regulatory Affairs