QUMAS is the leading developer of Enterprise Compliance Management Solutions designed to help regulated industries ensure regulatory compliance. For over a decade, QUMAS has been providing industry-proven Enterprise Compliance Management solutions to market leaders in the pharmaceutical, medical device, biotechnology, and contract research industry sectors. Using advanced technology and regulatory domain intelligence, QUMAS pre-packaged compliance management solutions automate critical document processes and dramatically reduce document cycle times. QUMAS solutions deploy rapidly to deliver FDA (including 21 CFR Part 11 (electronic signature and records)), EMEA and ISO-related best practices for the automation of controlled documentation and electronic regulatory submissions. QUMAS services include validation, user training, migration services and technical support as part of a total software and services offering.
