Reports when you need them.
Defensible, auditable, reproducible.
Toxicologists spend 60–80% of their time on evidence synthesis and report generation. Our products provide end-to-end automation delivering regulatory-grade risk assessments, OEL/HBEL reports, and REACH dossiers while keeping experts in control.
Backed by NIH, NSF, and EU research grants. Trusted by regulatory agencies, pharmaceutical companies, and research consortia.
An Integrated Platform
Three products that work together: curated data, intelligent analysis, and expert validation.
BioBricks
Data infrastructure
135+ curated datasets and growing. FAIR-compliant data infrastructure that powers our models and eliminates months of data wrangling.
ToxIndex
Automated assessment
Ask a question, get a regulatory-ready report. Specialized agents coordinate literature retrieval, database lookups, and models for metabolism, QSAR, ADME, and more, synthesizing evidence that would take a human team weeks to compile.
Sysrev
Expert validation
The human-in-the-loop. Toxicologists review and validate AI outputs, creating the audit trail and ensuring the accuracy that regulatory decisions demand.
See what a complete risk assessment looks like
Download a sample assessment or talk to our team about your use case.