Overview
This module provides in-depth knowledge of pharmacovigilance, focusing on the strategies and regulatory measures used to ensure the safety and effectiveness of pharmaceutical products. It covers the identification, assessment, and management of adverse drug reactions (ADRs), as well as the legal and ethical aspects surrounding drug safety monitoring.
Our Trainers
Mr. Sumet Hedao
CRO, Co-ordinator
Fortrea, Bangaluru, KA
Mr. Kalyani Patel
Process Lead
Alcon, Bengaluru
Ms. Sarani Dey
Subject Matter Expert- Pharmacovigilance
Cognizant, Bangalore
Ms. Shilpa Sharma
Process Lead
Alcon, Bengaluru
Modules
To start a professional career with understanding of principles of pharmacovigilance and drug safety
Learn the techniques used to identify and assess adverse drug reactions (ADRs).
Gain knowledge of regulatory frameworks and guidelines for drug safety.
Understand the working from respective experts and the way to pursue in PV field.
Outcomes
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Understand the Fundamental Concepts of Pharmacovigilance
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Identify and Assess Adverse Drug Reactions (ADRs)
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Apply Regulatory and Reporting Requirements
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Conduct Drug Safety Monitoring and Surveillance
