Documents & Resources
All essential materials in one place: AI documentation, practical materials, and additional resources to support your work.
Is Your Literature Review Missing AI Advantage
This one-pager helps pharmacovigilance professionals identify inefficiencies in their manual literature monitoring and shows how AI can streamline reviews, reduce workload, and improve accuracy.
Adverse Event Database from DrugCard
The document presents Adverse Event Database – a simplified, cost-effective ICSR management system with AI-assisted case creation, fast structured data entry, centralized case oversight, and flexible exports for audits and reporting.
Regulatory Intelligence Software from DrugCard
This file presents the Regulatory Intelligence tool, which centralizes global regulatory updates into a real-time, AI-summarized newsfeed with automated PDFs and fully customizable source monitoring.
How Automated Literature Monitoring from DrugCard Works
This document explains how DrugCard’s automated literature monitoring platform streamlines global journal tracking with AI-driven categorization, summaries, QC, and reporting — ensuring complete, audit-ready PV compliance.
platform features.
