Modern Drug Safety Reporting Starts Here.

AI-powered case management, built for global pharmacovigilance teams.

Process scanned reports, validate safety data, and meet FDA & PMDA deadlines—in minutes, not days. Never miss a compliance deadline.

Lower Costs. Higher Data Quality.
Better Compliance.

From handwritten reports in Japanese to scanned PDFs in English, our AI intelligently processes multilingual safety data and automatically generates region-compliant reports for the FDA, PMDA, or any global regulator

Conatus AI Demo - Japanese Pharmacovigilance Case Management Interface

How It Works

Extract

Auto-generate E2B data from unstructured data, including medical coding & narrative generation.

Validate

Auto-checks for completeness and consistency; flags issues for review or potential follow-up with the source.

Deliver

Outputs structured E2B data, ready for import into Argus or your existing system.

Share Globally

Auto-prepare a global view of the case with translation to meet global reporting requirements.

Human-In-The-Loop by Design

Automation accelerates your work, but never overrides your judgment. We deploy human review intelligently to QA the most important issues so you can meet compliance deadlines.

Enterprise-Grade Security for
Regulated Workflows

lock

HIPAA / APPI / GDPR compliant
Meet global data privacy requirements

shield

Data encrypted at rest and in transit
AES-256 encryption with TLS 1.3

assignment

Regulatory audit ready
Complete audit trails and documentation

business

Single tenant to isolate your data
Dedicated infrastructure for your organization

cloud

Flexible hosting options
Cloud, on-premise, or hybrid deployment with local data residency

group

Role-based access control
Granular permissions for different team roles

Join Our Early Access Program

We're partnering with a small group of forward-thinking PV teams to validate and shape the next generation of safety automation. Our Early Access Program lets your organization test and shape our solution at a minimal cost—you do not need to migrate from your existing software.

Zero migration. No commitment. Just results.

Frequently Asked Questions

Yes. We deliver structured outputs ready for systems like Argus or LifeSphere. Minimal changes required on your end.

Absolutely. Conatus supports workflows for both FDA and PMDA-specific requirements, including J-DSUR and EPPV.

Conatus balances automation with explainability and human QC. You stay in control and can intervene at any step.

All data is encrypted, with options for regional hosting. We meet global compliance standards for data privacy and auditability.