Zassi Medical Evolutions, Inc.
Like all medical device manufacturers, Zassi Medical Evolutions, Inc. must adhere to strict regulatory standards for manufacturing and quality, including FDA’s Good Manufacturing Practices and the 21 CFR 11 standard for their electronic records . When a medical device company does not comply, government levied fines can threaten its very survival.
Zassi was using an internal server-based application to handle their Quality System Record management. This solution was outdated, tied up staff
with unnecessary administrative and IT tasks, and was too expensive to upgrade.
Zassi wanted to manage their QSR and maintain compliance in the most flexible but painless way possible, and focus on providing innovative medical device technology to help patients. The company needed to manage detailed product data and minimize document control burdens.
