Our Technology
Purpose-built AI for pharmaceutical companies, medical device companies, and communication agencies for faster review, combining analytical precision with generative intelligence.
Hybrid AI Architecture
Our full hybrid AI model combines analytical AI with generative AI to deliver the gold standard in accuracy and hallucination control.
Linked, Anchored and Annotated Claims
Maintain always-current, searchable, validated libraries, with claims linked, anchored, and annotated so content can be reviewed against approved sources with full traceability.
Real-Time Prechecking
Instantly compare new content against approved libraries to identify deviations before MLR review begins.
SOC 2 Type II Certified
Enterprise-grade security with comprehensive controls protecting your sensitive pharmaceutical content.
AWS Bedrock Infrastructure
Built on secure, scalable cloud infrastructure with AI model inference contained within controlled boundaries.
Data Privacy First
Customer data is never used for AI model training without explicit written consent. Your content stays yours.
How It Works
Build your claims library
Approved content is automatically structured into a validated, searchable source.
Precheck new materials
New content is instantly compared against the library, deviations flagged before MLR ever sees it.
Focus your reviewers
The Quality Assessment Report surfaces only what needs attention, cutting review time per document.
MLR-ready submissions 70% faster — with fewer rounds of review.
2024 Pharmaceutical Technology Excellence Award Winner
Veeva AI Partner
Evaluating AI for MLR review?
Use our AI MLR Evaluation Checklist to compare solutions on accuracy, traceability, and security.
Agencies can also automate claim-to-evidence annotation with SecureCHEK AutoAnnotateSM.