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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Causality Assessment in PV: The Criteria and Category
Welcome to our blog, where we demystify the concept of causality assessment in the pharmacovigilance process. We understand that grasping the criteria and categories of causality assessment can sometimes be challenging. That’s why we’re here to simplify it for you, presenting the information in an easy-to-understand manner.
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❌ Counterfeit Drugs: An Adverse Event
In this comprehensive article, we delve into the world of counterfeit medicines. We explore what they are, how they are classified as adverse events, and the considerations involved.
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⚖ Understanding Civil Money Penalties
In this pharmacovigilance blog, we will delve into the details of civil penalties, addressing any uncertainties regarding the amount of penalties for late submissions or the provision of misleading data. Take a moment to read and gain clarity through this blog. Happy reading!
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🌎 Validating Incident Country: Key in Case Processing
Welcome to our informative pharmacovigilance blog, where we explore the significance of the country of incidence in ICSR (Individual Case Safety Report) case processing and its potential impact on the outcome of the case. Join in our journey through the world of pharmacovigilance.
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The Essential Role of Triage in Pharmacovigilance
Welcome to the next instalment of our blog series on case triage in pharmacovigilance, where we explore why triage is a crucial part of case processing. In this blog, we will provide you with a comprehensive understanding through the lens of triage.


