Tag: Basics of pharmacovigilance
Within this tag, you will delve into comprehensive insights about pharmacovigilance. This tag proves captivating as it precisely outlines the nuances of pharmacovigilance for your understanding.
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.•* MedDRA Coding: Core Principles Explained
n this MedDRA series article, we will explore additional tips to help enhance your case processing skills, particularly for those who may feel uncertain about MedDRA coding.
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Pregnancy cases in PV: An overview
In this comprehensive blog, you will explore the various categories and scenarios involved in handling pregnancy cases within pharmacovigilance case processing. Let’s dive in!
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📝 Decoding Personal Data in Pharmacovigilance Reporting
In this comprehensive blog, you’ll learn everything about handling personal data within pharmacovigilance reporting, along with crucial insights. Stay tuned for more updates!
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Off-Label Use: An Adverse Event
In this informative blog, you’ll explore into scenarios related to off-label use, learning how to assess them and accurately code them within MedDRA. Click to explore further details.
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㊙ Solicited Reports vs Unsolicited Reports: Key Differences
This blog provides specific information on: Introduction In this write-up, you will have clarity from: Many people believe in a wrong way that solicited and unsolicited refer to the sources of reports, but that is not the case. Here, you will find detailed explanations to help you understand these concepts. Definitions Solicited Reports: These reports…
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𒌐 CAPA Cases in Pharmacovigilance: An Overview
In this detailed blog, we explore into CAPA cases, their workflow, and their significance within pharmacovigilance. Explore further to gain a deeper understanding of how to effectively manage CAPA within this context.
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❇ Thalidomide incident and pharmaceutical industry
Welcome to our comprehensive blog where we delve into the transformative impact of thalidomide and its lasting influence on the cost burden of drugs in our society today. Gain a deep understanding of how the incident reshaped the way we approach drug development, testing, and regulation.
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Expedited Safety Reporting: Everything you need to know
In this blog, you will learn the term what is expedited reporting mean in the field of pharmacovigilance, including its standards and requirements. We delve into the time-frames associated with different types of reports, ensuring that you have a clear understanding of the urgency.
