About Pro Edriza Technologies

Pro Edriza Technologies Pvt. Ltd. is a pharmacovigilance company that works in two ways. As a contract research organisation we run drug safety operations for pharmaceutical, biotech and generic companies: case processing, literature monitoring, aggregate reports, signal management and regulatory submissions. As a technology partner we provide Edriza, our own pharmacovigilance platform, to companies that run safety in house.

What we do

• Individual case safety reports: intake, triage, coding, medical review, quality control and E2B(R3) submission to authorities and partners.
• Literature monitoring: local and global journal screening with full-text follow-up.
• Aggregate reports: PBRER, PSUR, PADER, DSUR and addenda, built from the case data.
• Signal management: detection, validation, assessment and tracking.
• Regulatory intelligence and submissions across the regions we cover.
• Audit-ready records: every action is recorded with who, when and why.

Where we work

India, the European Union, the United States, the United Kingdom, Canada, Japan, the Middle East, Asia and Australia, under ICH guidelines and the regional rules of each authority.