Pharm3r Information

About Pharm3r makes complex life sciences data accessible and actionable. Our PandoraPlus platform delivers post-market surveillance, adverse event analytics, regulatory intelligence, and supply chain risk monitoring to the world's leading life sciences insurers, pharmaceutical manufacturers, medical device companies, and legal and financial entities. Adverse Event Analytics — FAERS (13.6M+ cases) and MAUDE (13.5M+ reports) with real-time disproportionality statistics (PRR/ROR) benchmarked against product class norms ⚖️ Litigation Intelligence — Proprietary monitoring of plaintiff law firm websites as a leading indicator of emerging post-market safety risk 🏭 Supply Chain Risk — Regulatory action coverage across 93,000+ manufacturing facilities, with full product-to-facility hierarchy mapping 📋 Regulatory Intelligence — FDA warning letters, inspections, Form 483 citations, recalls, import refusals, and Health Canada regulatory records 🧪 Clinical Trial Analytics — 454,000+ trials from ClinicalTrials.gov, with trial arm adverse event cross-referencing 📊 Portfolio Management — Book-level exposure analysis for life sciences underwriters, with concentration risk visualization across products and product classes