European Drug Safety & AI 2026

24–25 Feb 2026 | Barcelona, Spain

ProductUpdated on 13 February 2026

Adverse Event Software for Efficient Safety Data Management | DrugCard

Head of Marketing at DrugCards

Ukraine

About

Adverse Event Software simplifies pharmacovigilance by providing an intuitive, enterprise-level database for entering, storing, importing, and exporting safety data with full ICH E2B(R2/R3) compliance. The platform centralizes all required fields, optionally integrates with DrugCard’s literature monitoring, and reduces manual work for faster case intake.

The system supports multi-format reporting with seamless conversion between E2B(R2) and E2B(R3), ensuring globally compliant safety operations. AI-powered signal detection highlights trends, identifies safety signals, and helps complete missing information, enabling quicker corrective actions.

Data integrity and compliance are guaranteed with FDA 21 CFR Part 11–certified electronic records and signatures, ISO/IEC 27001 and SOC 2 Type II–certified infrastructure, role-based access, and full audit trails. Advanced reporting includes CIOMS I/II, line listings, and ADR summaries, allowing fast export for regulatory-ready documentation.

Organisation

DrugCards

Estonia

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