PRISYM SaaS: A Compliance Ready Solution For Small To Medium Medical Device Organizations

Complying with FDA, EU and other regulations is a fact of life for medical device manufacturers and suppliers, irrespective of size or market sector. The burden of meeting these requirements is often most acutely felt in small to medium sized organizations that do not have the resources to implement the type of enterprise label lifecycle management solution that can automate much of the compliance process and reduce the load. PRISYM SaaS addresses this challenge for these smaller companies by enabling access to a compliance ready platform delivering high end capabilities for designing and controlling data oriented labels. Download the article for more information on the PRISYM SaaS.