Leading Swiss Pharmaceutical Company Goes Live with QUMAS Solution for Regulatory Submissions and Quality Management

QUMAS announced today that it has been selected by a leading Swiss Pharmaceutical company to provide an integrated end-to-end compliance platform. The company has implemented the QUMAS Compliance Platform across the entire organization to manage regulatory documents, change control, CAPAs, deviations, and electronic submissions to global regulators. QUMAS worked with the company to replace their legacy document management system, and to securely migrate all of their quality and compliance content into the new, integrated content and process management solution.


The QUMAS Solution allows the company to create, manage and securely store all regulatory and quality content and reports, as well as assemble content to be submitted electronically to regulatory agencies. The end-to-end compliance solution will be used by various departments (from clinical through manufacturing to sales and marketing) to automate and manage numerous processes including the recording and tracking of actions for CAPAs, deviations, change control, complaints and audits. The company also plans to implement the QUMAS’ learning management module to enable web-based training integrated with the compliance platform.



QUMAS is the leader in Enterprise Compliance Solutions with more than 270 global customer deployments and two decades of experience helping companies in highly regulated industries. QUMAS is a Microsoft Gold Partner, and provides the QUMAS Compliance Platform on SharePoint 2010, Documentum, Oracle or SQL. For more information, visit www.qumas.com.