|
|
- Eliminate manual document handling, printing, routing, storage, retrieval and associated time-loss and costs
- Author all validation documentation and templates in-application, without coding
- Standardize and lock-down validation records, protocols, and processes across an unlimited number of sites, globally
- Significantly reduce cycle-time for any validation lifecycle
- Execute testing online, applying 21 CFR Part 11/Eudralex Annex 11 compliant e-signatures
- Automate requirement and risk traceability
- Provide real-time validation status visibility and reporting
|
