Welcome to Your Journey as a Drug Safety Associate (DSA)

Congratulations!

You’ve taken a bold and essential first step toward a rewarding career in Pharmacovigilance by embarking on this Drug Safety Associate (DSA) training. In a competitive job...

INTRODUCTION: 

Understanding the key terms in Pharmacovigilance is critical for accurate communication, case processing, and regulatory compliance. This course provides an in-depth exploration of terminology related to ICSR types, processes,...

The Building Blocks of Your New Career

Mastering the sources of Individual Case Safety Reports (ICSRs) is a crucial step in your Pharmacovigilance journey. By understanding where ICSRs originate and how data is gathered, you’ll gain the skills...

The Building Blocks of Your New Career

As a Drug Safety Associate, your ability to effectively manage Individual Case Safety Reports (ICSRs) is critical to ensuring patient safety and regulatory compliance. This course focuses on the essential...

Overview:

This advanced course delves into the methodologies and principles of causality assessment in Pharmacovigilance, equipping learners with the knowledge and skills to determine the relationship between a drug and an adverse event. By...

Overview:

This advanced course equips learners with the technical and practical skills required for writing clear, concise, and comprehensive ICSR narratives. It focuses on the structure and components of narratives, best practices to ensure...

Overview:

This advanced course provides a comprehensive understanding of safety databases used in Pharmacovigilance. It focuses on technical aspects of case processing, including case entry, follow-up, duplicity checks, and database management....

Overview:

This advanced course provides a deep dive into the essential coding systems used in Pharmacovigilance—MedDRA (Medical Dictionary for Regulatory Activities) and WHO-Drug. It focuses on understanding the structure, hierarchy, and...

Overview:

This expert-level course focuses on the critical role of literature monitoring in Pharmacovigilance, highlighting its importance in identifying adverse events and ensuring compliance with global safety reporting regulations. It covers...

Overview:

This expert-level course focuses on the critical aspects of regulatory reporting in Pharmacovigilance, highlighting the importance of accurate and timely reporting of adverse events to regulatory authorities. The course covers expedited...