Electronic Document Management Solutions for Life Sciences

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:

For more information on the QUMAS eDMS capabilities for your industry, go to

Alternatively, check out this Quality Assurance Documents Package from the QUMAS Packaged Solutions, which offers an off-the-shelf approach to SOP Management.