Certificate Course in "Pharmacovigilance Practical ICSR"

Practical ICSR, Case Validity, MedDRA in ARGUS, Seriousness assessment, Causality assessment, Case processing in ARGUS.
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Certificate Course in "Pharmacovigilance Practical ICSR"
699
students
3.5 hours
content
May 2023
last update
$19.99
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Why take this course?

🚑 Certified Course in "Pharmacovigilance Practical ICSR"

🚀 Headline: Master the Art of Pharmacovigilance with Real-World ICSR Scenarios! 🚀


Course Overview:

This course is a natural progression from our foundational "Basic ICSR" course, delving deeper into the practical application of pharmacovigilance principles. It's designed to equip you with hands-on experience and the necessary skills to excel in the field.


🧭 Practical ICSR: A Deep Dive into Case Management 🧭

  • Introduction to ICSR: Gain a solid understanding of what an Individual Case Safety Report (ICSR) is and its importance in drug safety.
  • Our Training Objective: This development course is crafted to include practical case scenarios, guiding you to apply theoretical concepts into practice effectively.
  • Training Benefits:
    • Practical Application: Learn to apply your ICSR knowledge through real-world examples and live MedDRA access.
    • Enhanced Skills: Develop logical thinking and critical evaluation skills for assessing and processing cases.
    • Case Prioritization: Understand the nuances of prioritizing cases based on their potential impact.
  • Topics Covered:
    • ICSR Fundamentals: Dive into the basics of ICSRs, including case validity, duplicate detection, event selection, and coding with MedDRA.
    • Assessments: Learn how to assess seriousness, labelling, and causality, essential steps in the ICSR process.
    • Narrative Writing: Perfect your narrative writing skills, which are crucial for accurate reporting.
    • Practical Scenarios: Engage with a variety of case scenarios that challenge and enhance your learning experience.
  • Case Prioritization Rules: Understand the criteria for prioritizing cases and meet regulatory authority submission timelines.

**🔍 Instructor Spotlight: Srikanth Gorantla 🔍

With over 10 years of experience in Pharmacovigilance, our course instructor, Ramya Mam, is an expert in ICSR processing, literature search, signal assessment, and aggregate reporting. Her extensive knowledge and real-world expertise will guide you through this course with a focus on practical learning.


Why Choose This Course?

  • Real-World Focus: This course is tailored to provide hands-on experience with pharmacovigilance, focusing on real-world case scenarios.
  • Live MedDRA Access: Gain direct access to MedDRA terminology, which is crucial for accurate coding and reporting of adverse events.
  • Expert-Led Instruction: Learn from an instructor with a wealth of knowledge and experience in the field.
  • Skill Development: Enhance your ability to critically evaluate, prioritize, and handle complex ICSR cases effectively.
  • Comprehensive Learning: From case validity to narrative writing, this course covers all aspects of pharmacovigilance handling.

🎓 Key Learnings 🎓

By the end of this course, you will have a clear understanding of how to manage and assess ICSRs, apply MedDRA terminology, perform seriousness and causality assessment, write narratives for case reporting, and prioritize cases according to their urgency. You'll be well-equipped to navigate the complex world of pharmacovigilance and contribute meaningfully to drug safety.


📝 Checking for Understanding 📝

This course is designed not just to inform but also to test your understanding of the material covered. Through interactive assessments and practical exercises, you'll demonstrate your ability to apply what you've learned in real-world scenarios.


Join us on this journey to become a proficient professional in the field of Pharmacovigilance through our "Certified Course in 'Pharmacovigilance Practical ICSR'". Your expertise in drug safety starts here! 🕊️✨

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5336972
udemy ID
20/05/2023
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26/05/2023
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