Precision-driven solutions for regulatory excellence and patient safety
Cross-verify safety databases against source records. Identify gaps, duplicates, and compliance risks with precision mapping.
Validate data integrity before, during, and after database migration. No lost cases. No audit surprises.
Licensed MedDRA subscriber. We offer standalone coding for AEs, indications & medical history, plus version upgrades with full traceability.
Bulk-correct narratives, coding, causality, and seriousness fields from inherited backlogs at scale with automated validation.
One missed article can mean one missed signal.
Published literature is often the first place emerging safety issues surface—before they reach your database, before regulators flag them, and before they become crises.
Effective literature screening isn't optional—it's a regulatory mandate and a critical early warning system. ADRs, efficacy concerns, off-label use patterns—they're all hiding in plain sight across thousands of journals, conference abstracts, and regional publications.
We don't just search. We find. Drugvigil delivers systematic, audit-ready literature screening across indexed and non-indexed sources—globally and locally—so nothing slips through.
We provide a range of services including:
Poor pharmacovigilance isn't just inefficient—it's dangerous. These are the risks that cost companies millions in penalties, damage reputations, and put patients at risk.
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We are Drugvigil (pharmacovigilance service provider) headquartered in India. We also do our limited operations at Tbilisi, Georgia. We help pharmaceutical companies and healthcare professionals improve the safety of their products.
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