Evidence-Sensitive Workflows
Designed to Support Regulated and Evidence-Sensitive Workflows
TARE helps teams produce clearer records, stronger provenance, better audit evidence, and more reviewable documentation for teams preparing audit-ready lab records.
Designed to support 21 CFR Part 11 concepts
Designed to support GxP-style documentation practices
Designed to support ISO/IEC 17025-style evidence expectations
Supports data integrity principles such as attributable, legible, contemporaneous, original, accurate, complete, consistent, enduring, and available
Compliance support model
TARE helps organize records, evidence, approvals, and exports so quality and compliance teams can review work with better context.
Validation scope, SOP approval, and quality-system signoff stay with the customer's responsible teams and reviewers.