Pharmacovigilance Blog

ICSR Management

A Newcomer’s Guide to ICSR Case Processing Workflow

This is a very late blog in this particular category, where we dive into the step-by-step process of ICSR (Individual Case Safety Report) case processing. Whether you are new to the field or seeking a refresher, this blog is designed to provide you with a comprehensive understanding of the process.

Bala

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Talk About Quality

Quality Upgrade: Simple Hacks for Seamless Case Processing

Welcome to our ICSR hacking blog focused on quality. In this article, we explore simple and easy daily routine of methods to enhance the quality of case processing. Rather than relying on discussing and gossiping, we draw from real-world experiences to provide you with logical insights and actionable tips. #Blog/Excerpt

Bala

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Drug safety and pharmacovigilance

Understanding Day-Zero(0) in Pharmacovigilance

In this comprehensive blog, you’ll uncover key information about what “Day Zero” signifies in the context of case processing and the broader field of pharmacovigilance. Additionally, you’ll gain insights into calculating the day of submissions.

Bala

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Who & When & How

Understanding Root Cause Analysis

This is a serious of blog explaining the associated processes, From this you will gain a knowledge on handling Root Cause Analysis in general way and explaining of implementing in your workplace.

Bala

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Drug safety and pharmacovigilance

Challenge Assessments: Exploring Dechallenge and Rechallenge

In this detailed blog post, we explore into the intricate differences between the terms “dechallenge” and “rechallenge,” providing key considerations. Learn deeper by clicking here.

Bala

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ICSR Management

Understanding invalid composite case

Welcome to our informative blog, where we shed light on a lesser-known aspect of case processing: the invalid composite case. In this article, we provide a comprehensive exploration of this particular type of case and its significance within pharmacovigilance. Whether you are already familiar with it or encountering this concept for the first time, we aim to offer detailed insights and explanations.

Bala

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MedDRA Series

Challenges in MedDRA Coding: Identifying Common Causes

From this comprehensive enlightening blog, you will learn about crucial aspects frequently encountered during MedDRA coding, which often result in frequent action items and errors. Read on to explore further.

Bala

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Exploring Adverse Events

Examining LOE cases in Pharmacovigilance

In this comprehensive article, we delve into the specifics of “LOE” (Lack of Efficacy) within the context of adverse events. We explore distinct scenarios to differentiate between what constitutes LOE and what does not.

Bala

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