Electronic Document Management Software

Regulations mandate effective content control, and Pharmaceutical and Biotech organizations recognise the need to have easy to use Document Management Solutions. For many employees, the requirement to access their DMS is a daily requirement and they need to have fast, easy access to an intuitive system that meets 21 CFR Part 11 requirements.

In the Quality Assurance arena, users need a solution that allows for strong version control and audited distribution of SOPs to ensure that only the latest versions are in circulation and users are properly trained on the correct procedures. These documents may require printing in which case strict print controls become an important feature as well.

For more information on a Platform approach to the management of content across the lifecycle of drug discovery and manufacturing, watch this webinar Regulatory Affairs and Quality Assurance Compliance on a Single Platform.

Or download this webinar for information on Qualifying SharePoint 2010 and Delivering a 21 CFR Part 11-Compliant Quality Management Solution.