Pharmacovigilance Blog

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.

Bala

Read

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…

Bala

Read

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.

Bala

Read

Literature Screening

Open-Source Literature Review: A Practical Guide

A practical guide to open-source literature review, highlighting free tools and workflows to streamline research from search to systematic review.

Bala

Read

Talk About Quality

IDMP Standards Explained: Importance and Benefits for Clinical Projects

This article explores the importance of IDMP standards in clinical projects and highlights the key benefits they bring to data consistency, regulatory compliance, and global information exchange.

Bala

Read

Drug safety and pharmacovigilance

What are IME listings?

This article provides an overview of Important Medical Event (IME) listings, their development, and their role in pharmacovigilance.

Bala

Read

ICSR Management

Causality Classification in Pharmacovigilance: Explained

A simplified guide to causality assessment in pharmacovigilance, covering WHO-UMC classifications and key criteria for evaluating adverse drug reactions.

Bala

Read

Drug safety and pharmacovigilance

Compliance for Beginners: Pharmacovigilance

This article simplifies key compliance concepts, highlights practical do’s and don’ts, and provides essential insights to help case processors and newcomers.

Bala

Read