DrugCard

DrugCard automates pharmacovigilance — from global and local literature monitoring to regulatory tracking and case management. Cost-effective, regulatory-compliant, and powered by AI. We help PV teams save time, stay compliant, and never miss a safety signal.

Key Products
— Literature Monitoring
Automated monitoring of PubMed and 2,200+ local journals across 121+ countries in 100+ languages.
— Regulatory Intelligence
Centralized tracking of regulatory updates from global and local health authorities.
— Adverse Event Database
Intuitive safety case management — collect, assess, and track adverse events in one audit-ready platform. Includes AI Case Intake: automatic extraction of adverse drug reaction data from unstructured text (powered by LLM, launched December 2024).
— SimpleSearch
Free tool for instant global literature search — no setup or subscription required.
— eCTD Light Documentation
Streamlined module for regulatory submission document management.