News Bulletin for August 28, 2014; QUMAS, a leader in regulatory, quality and compliance management solutions, today announced that a leading Japanese pharmaceutical company, has selected QUMAS DocCompliance to manage and control quality documents across facilities located in Japan, North America, Asia, and Europe. The QUMAS solution is currently being used by 400 employees and will be rolled out to an additional 1,850 employees by the end of 2014.
QUMAS DocCompliance provides the company with a complete web-based electronic document management system that enables users to create, distribute, and manage Standard Operating Procedures (SOPs) across the business. The QUMAS solution assures compliance with all cGxP requirements for procedure management and supports Electronic Signatures as per the FDA 21 CFR Part 11 requirements. NetDimensions, a QUMAS technology partner, will provide an integrated learning management system that will ensure that all users are properly trained on all relevant policies and procedures. All of the capabilities of QUMAS DocCompliance and the NetDimensions learning management system are accessed seamlessly through MyQUMAS, a user-friendly portal interface.
“By standardizing on our solution across the organization, employees will have immediate access to the most recent SOPs,” stated Caoimhe Kiely, Vice President of Marketing at QUMAS. “Additionally, users will be able to collaborate in a compliant manner when creating or updating documents.”
QUMAS, now part of BIOVIA from Dassault Systèmes, is the leader in Regulatory, Quality, and Compliance Management Solutions with more than 280 global customer deployments and two decades of experience helping companies in highly regulated industries. QUMAS is a Gold Microsoft Partner, and provides the QUMAS Compliance Platform on SharePoint, EMC Documentum, Oracle or SQL. For more information, visit www.qumas.com.
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