Document Control Capabilities

Configuration aligned with FDA 21 CFR Part 11 and EU GMP Annex 11 requirements.

Operational Outcomes

Commercial Impact and Supplier Performance

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Current effective documents prevent quality complaints and OOS/OOT incidents caused by outdated work instructions.

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Audit-Ready Document Control for Microsoft 365

ValidaPoint configures Microsoft 365 as a GxP-compliant document control system. Typical deployment: 8 weeks.
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Need to Establish Audit-Ready Document Control?

ValidaPoint configures Microsoft 365 as a GxP-compliant document control system. Typical deployment: 8 weeks.