Document Control Capabilities
Configuration aligned with FDA 21 CFR Part 11 and EU GMP Annex 11 requirements.
ValidaPoint configurations reduce operational errors, minimize corrective action plans (CAPAs), and protect strategic customer contracts during Supplier Performance Evaluations.
Obsolete Document Findings
Automated version control and print restrictions eliminate the most common GxP audit observation.
Audit Traceability
Standardized configuration protocols establish a fully defensible, validated system that holds up under direct regulatory scrutiny.
Data Sovereignty
All files, metadata, and audit trails remain within your own Microsoft 365 tenant.
Approved Supplier Status
Current effective documents prevent quality complaints and OOS/OOT incidents caused by outdated work instructions.


