Qumas, a provider of enterprise compliance technologies, has signed a contract to supply an integrated compliance platform to a Swiss pharmaceutical company for regulatory submissions and quality management.
The company leverages the technology to manage regulatory documents, change control, CAPAs, deviations, and electronic submissions to global regulators at various departments.
Implemented across the entire organization, the Qumas Compliance Platform replaced the company's legacy document management system and the quality and compliance content was securely migrated into the new, integrated content and process management technology.
All the regulatory and quality content and reports can be created, managed and securely stored using the technology, besides assembling content to be submitted electronically to regulatory agencies.
The technology is designed to automate and manage processes such as the recording and tracking of actions for CAPAs, deviations, change control, complaints and audits.
Further, the Qumas' learning management module is expected to be implemented by the company for web-based training integrated with the compliance platform.
