ProcessCompliance Datasheet - Pharmaceutical Business Review

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Published 12 May 2011 | By QUMAS

QUMAS ProcessCompliance™ enables organizations to standardize and automate their business processes that manage the collection, tracking, and analysis of information and the resolution of related issues. ProcessCompliance includes web-based, configurable processes, workflows and forms that can be tailored to meet the needs of the organization. ProcessCompliance integrates with QUMAS DocComplianceTM to provide access to controlled documentation during all phases of process management and with QUMAS ComplianceUnityTM for sophisticated reporting of their business performance. Organizations not only benefit from an increase in efficiency and accuracy of business processes and activities, but also proactively improve their business performance.

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R&D Submission Documents Package QUMAS offers a number of Packaged Solutions providing pre-defined and pre-tested configurations of Document content management or Process management for specific, common industry problems. This Package addresses document management requirements around documents used in Global Regulatory Submissions, particularly CTD and eCTD submissions. The pre-defined configuration supports the creation, approval, and ongoing lifecycle management of documents used in functions such as Clinical, Nonclinical, Quality, Manufacturing, Regulatory Affairs, and Safety. Products

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