DrugCards

DrugCard provides a cost-effective and regulatory compliant platform that automates pharmacovigilance — from global and local literature monitoring to regulatory tracking and case management. We help PV teams save time, stay compliant, and never miss a signal. Powered by AI, DrugCard transforms complex data into actionable insights, automates reporting and literature screening, and allows experts to focus on what matters most — strategic decisions and patient safety. Automated Local and Global Literature Monitoring Monitor both global databases like PubMed and local journals in one place. We already cover 104+ countries and 1800+ local journals, and counting. We add any journal you need — fast and without bureaucracy. No missed publications. No manual searches. Just faster, safer pharmacovigilance. AI-Powered Regulatory Intelligence Receive updates from global and local authorities in one centralized view — no more checking dozens of websites manually. DrugCard keeps your team informed on every regulatory change so you can act fast, stay compliant, and focus on what’s next — not on chasing updates. Adverse Event Database & Software Manage safety cases with an interface that feels intuitive, not overwhelming. Get the full “enterprise” functionality without the complexity, cost, or six months of training. Everything you need to collect, assess, and track adverse events efficiently — all in one secure, audit-ready platform. Pharmacovigilance Services Extend your in-house capabilities with our PV specialists. DrugCard combines automation with human expertise — from literature review and reporting to quality checks and documentation. You get precision, consistency, and compliance delivered by experts who understand your needs.