Pharmacovigilance Blog

MedDRA Series

MedDRA Encoding and Auto-Encoding: Key Considerations

This article explores the fundamentals of MedDRA encoding, the role of auto-encoding, & common pitfalls that every pharmacovigilance professional should understand.

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Drug safety and pharmacovigilance

E2B Cases: Classification, Differences, and Processing Explained

This blog features: Introduction If you work in a Drug Safety or Pharmacovigilance department, you have likely come…

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Public Authorities and Safety

Why VigiBase Matters: The Backbone of Global Pharmacovigilance

This article explores the structure, importance, statistics, & critical role of VigiBase in protecting public health through international PV collaboration.

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Public Authorities and Safety

SUGAM Portal: Complete Guide to CDSCO’s Online Regulatory System

This article provides a complete overview of the SUGAM portal, its purpose, major applications, key features, and its importance in India’s clinical ecosystem.

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ICSR Management

SAR vs SAE in Pharmacovigilance: Definitions, Differences, & Key Concepts

This article explains the definitions, highlights the critical differences between SAR and SAE, and explores the key concepts in pharmacovigilance.

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Techs & Tools

Enhancing Pharmacovigilance with NLP and Text Mining

This article provides an overview of NLP applications in pharmacovigilance, including literature review, data extraction, AE identification, and annotations.

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Exploring Adverse Events

FDA FAERS Analysis: Rising Trends in Serious Adverse Events Reports

This blog features: Introduction In this article we discuss about the trends of adverse event reporting which are…

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ICSR Management

Country Attribution in ICSRs: Rules, Challenges, & Best Practices

A quick guide to country attribution in ICSRs and their role in ensuring accurate, compliant safety reporting.

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