GxP Data Integrity
21 CFR Part 11 demands ironclad electronic records. We automate the technical verification of Every batch record, deviation, and CAPA.
21 CFR Part 11 Validated AI
Life Sciences Precision
The highest standard of operational integrity. We automate the verification of batch records, master formulas, and GxP documentation for the world's most regulated facilities.
Zero-Defect Operations
Pharmaceutical manufacturing requires absolute data integrity and continuous audit readiness.
Validation Scaling
Accelerating computer system validation and equipment qualification. We turn the validation burden into an automated competitive advantage.
Continuous Audit
Transitioning from "audit prep" to "always ready." Instant access to complete technical lineages for every ingredient and process step.
Pharmaceutical Intelligence
AI engines specialized for high-stakes GxP environments and infinite technical data lineages.
Comprehension Engine
Query your entire validated specification database and GxP library. Get instant answers for clinical lineage and regulatory inquiries with full traceability.
Learn moreDocument Intelligence
Process COCs, COAs, and supplier validation packages automatically. Scale your document review process while maintaining absolute data integrity standards.
Learn moreIntelliSync MSS
Maintain the highest pharmaceutical sanitation standards with predictive scheduling. Audit-ready technical packages for every cleaning and maintenance event.
Learn moreProven in the Toughest Trenches
Built and proven in the Food & Beverage industry—one of the most heavily regulated sectors on earth. We bring that same operational rigor and data integrity to Pharmaceutical and Life Sciences manufacturing.
100%
Traceability
21 CFR
Part 11
GxP
Compliant
See What's Possible in Pharmaceutical & Life Sciences
Schedule a personalized demonstration of how our AI solutions can optimize your workflows.