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.
How to Choose the Best Software for Literature Monitoring – A Practical Checklist
This practical checklist for pharmacovigilance teams to evaluate and compare literature monitoring software, covering compliance, AI features, usability, security, and scalability.
Pharmacovigilance Literature Monitoring Pre-Audit Checklist
Adequate preparation for a pharmacovigilance audit requires careful planning and a structured approach. Using a Pharmacovigilance Literature Monitoring Checklist allows PV teams to assess their processes, identify gaps, and ensure they are fully prepared for an audit.
Pharmacovigilance services by DrugCard
This document outlines DrugCard’s end-to-end pharmacovigilance services, delivered with minimal client effort and full regulatory compliance.
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