Category: ICSR Management

This article demystifies the distinction between the two, the terms why severe isn’t always serious are often misunderstood—and mistakenly used interchangeably.

In this comprehensive blog discussing data entry into databases, we will explore essential factors to consider and apply when dealing with Adverse Event coding. Check this out.

This blog covers: Introduction In this blog, we explore how report types can vary depending on the reporter, and conversely, how the reporter can often be inferred from the type of report submitted. While this isn’t a strict rule, it provides useful insights into how reports are typically classified and understood within case processing. Reports…

This blog covers: Introduction If you’re involved in case processing, you’re likely aware that investigation records can sometimes be classified as adverse events or part of the medical history. This blog, we discuss this topic with a focus on helping beginners understand the nuances, including some important coding conventions for capturing significant investigation findings as…

This blog features: Introduction Many pharmacovigilance professionals experience a range of uncertainties when it comes to the process of case nullification. One common scenario is identifying a duplicate case but not knowing which one should be nullified and which should be retained. To address this confusion, this guide provides clear direction on case nullification, highlighting…

This blog covers: Introduction Have you ever wondered how to merge cases effectively without compromising important information? In this comprehensive blog, we’ll guide you through the essential checklist to follow during the case merging process — from the initial steps to the key indicators you need to monitor along the way. Whether you’re just starting…