Best Practices for Pharmacovigilance Systems Training Course

Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problems. Then the critical question to ask is how do you go about achieving this? This course is designed to provide you hands on learning on how to manage and conduct drug safety monitoring, perform post-market Pharmacovigilance, detect drug safety signals, improve drug safety or create new products & services and assess, manage and mitigate risks. World Health Organization (WHO) defines Pharmacovigilance as “the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other possible drug-related problems”. In this course you shall learn the approaches and techniques to enhance drug safety and patient outcomes by leveraging Adverse drug reaction reporting systems, post-market Drug safety intelligence.and learn the approaches on how to collect, track, analyze Adverse Drug Reactions (ADR's), Individual Case Safety Reports (ICSR's) and how to prevent, reduce or eliminate medications errors.

Upon completion of this course, you should walk away with:

• Objectives of Pharmacovigilance
• What are the best practices of Pharmacovigilance?
• Understanding the key deliverables of Pharmacovigilance
• Need of Risk Assessment and Risk Management System
• Continuous Drug Safety Monitoring
• Individual Case Safety Reports
• Adverse Drug Reactions
• Identifying Product-Event Combinations
• Premarketing Risk Assessment
• Postmarket Risk Assessment
• Identifying and Detecting Safety signals
• Improving Drug Quality