Tag: All about ICSR processing
Within this tag, you will discover a complete repository of information pertaining to ICSR (Individual Case Safety Report) cases, presented systematically from top to bottom at each level.
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👥 Mastering Duplicate Detection: Your Ultimate Guide
In this detailed blog, we delve into the detection of duplicates in pharmacovigilance case processing, incorporating statistical insights throughout our exploration. Join us on our journey as we share our findings and insights.
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➕ Understanding Duplicates in Pharmacovigilance
This blog covers: Introduction Duplicate reports are a regular challenge in pharmacovigilance case processing, encountered by professionals. This blog aims to gain a understanding of duplicates and their global impact on pharmacovigilance datasets. We’ll discuss methods for: What Are Duplicates? Duplicates refer to where a case file exists in many versions, that contains similar information…
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101: Effective Case Book-in Pharmacovigilance: A Step-by-Step Guide 🎟️
Here in this informative pharmacovigilance blog, where we provide a comprehensive overview of the book-in process in Individual Case Safety Report (ICSR) management. In this article, we present a step-by-step guide that simplifies the book-in process, ensuring a better understanding for all.
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📛 Medication Error: An Adverse Event
Discover crucial information on medication error and drug safety in Drugvigil’s blog. Stay informed on pharmacovigilance updates.
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🏁 Case Processing: Initials and Follow-ups Explained
This blog includes: Introduction In adverse event reporting, each case often includes initial reports and multiple follow-ups. This can lead often confusion, when trying to locate the report you are processing. This guide aims to clarify these terms and help you navigate through the complexities of reporting. Definitions Initials Initial reports are the first submissions…
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🪪 Listedness and Labelling: Explained
This blog covers: Introduction This blog focuses on the processes involved in conducting causality assessments. You will learn about the distinctions between two terms in this context: listedness and labelling, along with their interconnections. Listedness Listedness refers to the recorded terms derived from pre-clinical study data. In which encompass monitored and documented events related to…
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🗓️ Picking Receipt Dates For Various Scenarios
In this article, you’ll learn how to picking receipt dates during case processing in various scenarios—a commonly confusing aspect. We will explore the complexities involved and provide clarity on this often intricate topic.
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🥨 E2B and E2B(R2) and E2B(R3): The Variations
Welcome to our informative blog. Here you can learn about the difference between E2b (R2) and E2b (R3), Building upon our previous discussion about E2B, we now delve deeper into the evolution of the E2B standard.
