Validated Web-Based Application Cuts Customer Costs by Over 90%
San Diego, CA: GxPReady!, a company that provides SaaS applications for use in FDA regulated industries, has completed validation of GxPReady! Suite. This product is a SaaS software application qualified to meet FDA regulations for tracking calibration, validation, and maintenance activities. Pharmaceutical, biotech, and medical device companies that adopt this product reduce their cost of meeting regulatory requirements by up to 90% compared to the current industry practice of qualifying software in-house.
“GxPReady! Suite is a great product for small and mid-sized FDA regulated companies”, explains GxPReady! CEO Vince Sebald, “they can be up and running with a quality, validated system in a few weeks or less. Usually, this would take up to a year or more. And, since it is affordable for even small companies, compliance can be achieved earlier than would otherwise be practical. It’s just a more efficient way to be compliant. We are very excited to provide this option to the FDA regulated industry sector.”
GxPReady! is a privately owned software development company based in San Diego, California, dedicated to developing web-based validated applications to support FDA regulated customers including pharmaceutical, biotech, and medical device manufacturers and support facilities. It has developed a proprietary validation technology to virtually eliminate validation of applications by the users of applications using this technology.