Electronic Document Control and Management are the cornerstones of Quality and Compliance in Life Sciences.
The QUMAS solution for Electronic Document Management (EDM) delivers proven regulatory compliance practices for document control and related training across the business. Delivering compliance with FDA 21 CFR Part 11 including Electronic Signatures and Audit Trail, SOP management, Policies, Procedures, Work Instructions, Manuals, Files and Reports will be created and controlled in compliance with global regulatory mandates.
Download the following webinars for solution and capability overviews:
- Looking for an Electronic Document Management - Start Here
- Why does your organization need an electronic Quality Management System?
- Best Practice Deviation, CAPA, and Change Control with BIOVIA QMS
- SharePoint 2013 as a QMS for Controlled Documents & Quality Processes
- Your brand new EQMS is Electronic, Automated, and Efficient. But is it Intelligent?
For more information on the QUMAS eDMS capabilities for your industry, go to