Document Management for Life Sciences
AODocs' quality management system helps you simplify your GxP and FDA Title 21 CFR Part 11 compliance processes, accelerate internal innovation, and secure your data. With a user-friendly content management system that makes information easy to access and share, you’ll be able to release your products faster.
Improve collaboration and increase innovation by allowing users to work in a user-friendly environment while also cost-effectively expanding your audit, CAPA, and bill of materials capabilities.
21 CFR Part 11 compliance
Manage your controlled documents using change request workflows that are backed up by full audit logs to help you stay compliant with FDA Title 21 CFR Part 11.
Stay fully compliant with controlled, validated releases, two-factor authentication for approvals, a post-processed audit log, supporting documentation, and technical support.
Pull business insights
Get a global view of your documents, their workflow statuses, and user activity with comprehensive dashboards. You can also quickly identify problem areas in advance of an audit, track progress, and identify bottlenecks in your processes.
Maintain data integrity
Maintain complete, attributable records of all your data, store and track document metadata, and leverage Google’s best-in-class security and compliance controls.
IT Manager, Ceva Animal Health
"Tracking the registration of new products via paper was too much work. We wanted to digitize everything. AODocs has improved the productivity of the team by nearly 100%, while reducing the risk of costly human errors."
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