Transform YourPV Reporting Workflow

PV-Submit is an end-to-end pharmacovigilance submission assistant designed to streamline safety reporting workflows with advanced AI technology.

Pharmacovigilance workflow diagram

Advanced AI Engines

Our three specialized AI engines work together to streamline your pharmacovigilance workflow.

Auto-Summarizer
Instantly convert raw case data into compliant medical narratives with our advanced AI engine.
Coding Assistant
Apply accurate MedDRA and WHO-DD codes automatically with our intelligent coding system.
Submission Formatter
Generate submission-ready packages such as E2B(R3) XML and CIOMS forms for FDA, EMA, and other regulators.

Why Choose PV-Submit

Transform your pharmacovigilance workflow with these powerful benefits.

Streamlined Reporting

Reduce the time spent on manual data entry and report generation by up to 80%.

Enhanced Accuracy

Minimize human error with AI-powered coding and formatting that follows regulatory guidelines.

Regulatory Compliance

Stay compliant with FDA, EMA, and other global regulatory requirements with automatically formatted submissions.

Audit Readiness

Maintain comprehensive audit trails and documentation for all submissions and changes.

Seamless Integration

Easily integrate with existing pharmacovigilance systems and databases.

Time and Cost Savings

Significantly reduce processing times and operational costs associated with safety reporting.

Ready to transform your workflow?Start using PV-Submit today.