Manage Your Critical Content
With the array of required documentation, regulated businesses drown in paperwork – whether it’s printed or digital. Reduce compliance risks, improve product submissions and increase the speed and quality of product development and manufacturing lifecycles by effectively managing your information.
Managing your content is complex and difficult, but a necessity. FDA 21 CFR Part 11 has a broad impact on content, since it affects electronic records, including Word documents, spreadsheets and graphics.
A comprehensive content management solution enables you to:
- Share information quickly and easily
- Produce quality business intelligence
- Improve productivity and efficiency
- Operate in a more compliant state
- Reduce duplication of efforts
- Put the right information in hands of the right decision makers
InfoStrength Tames the Information Flood:
Create intelligent documents that become accurate, consistent templates for regular business operations.
Store your data in a trusted centralized location to make finding and sharing information easy. This is critical when your content is subject to regulation.
Move and track information from creation, to management, to sharing, to publication and finally to archiving. Easily identify original documents, versions and authorized users.