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The Certificate Course in Pharmacovigilance offers an in-depth exploration into the critical role of drug safety monitoring in the healthcare industry. Throughout this month-long program, participants will engage with the fundamental concepts of pharmacovigilance, including adverse event reporting, risk management, and data analysis. The course is designed to blend theoretical knowledge with practical skills through case studies, regulatory document reviews, and real-world data evaluation exercises.
The Certificate Course in Pharmacovigilance offers an in-depth exploration into the critical role of drug safety monitoring in the healthcare industry. Throughout this month-long program, participants will engage with the fundamental concepts of pharmacovigilance, including adverse event reporting, risk management, and data analysis. The course is designed to blend theoretical knowledge with practical skills through case studies, regulatory document reviews, and real-world data evaluation exercises.
This program aims to provide comprehensive training in pharmacovigilance principles and practices, focusing on the monitoring, assessment, and prevention of adverse effects associated with pharmaceutical products. Participants will learn to ensure drug safety and compliance with global regulatory standards, enhancing patient care and public health outcomes
PhD in Computational Mechanics from MIT with 15+ years of experience in Industrial AI. Former Lead Data Scientist at Tesla and current advisor to Fortune 500 manufacturing firms.
Professional Certification Program
Week 1: Introduction to Pharmacovigilance and Drug Safety
Definition, objectives, and global importance of pharmacovigilance
Historical evolution and landmark drug safety incidents
Types and classification of adverse drug reactions (ADRs)
Overview of drug development lifecycle and regulatory checkpoints
Week 2: ADR Reporting Systems and Regulatory Frameworks
Spontaneous reporting systems: WHO-UMC, Vigibase, MedWatch
Pharmacovigilance guidelines (ICH, EMA, CDSCO, FDA)
Signal detection and risk assessment methods
Data mining techniques in safety surveillance
Week 3: Advanced Pharmacovigilance Tools and Technology
Case processing and narrative writing (ICSRs, PSURs)
Pharmacovigilance software: Argus, ARISg, Veeva Vault Safety
Integration of AI, machine learning, and automation in drug safety
Data visualization and dashboards for safety signal analytics
Week 4: Career Pathways, Compliance, and Future Trends
Roles in PV: Drug safety associate, quality reviewer, risk assessor
Audit, inspection readiness, and pharmacovigilance compliance
Global outsourcing and PV operations in India
Emerging trends: Real-world evidence, mobile reporting apps, and predictive PV models
Standard Fee: INR 8,998 USD 198
Discounted Fee: INR 4499 USD 99
We are excited to announce that we now accept payments in over 20 global currencies, in addition to USD. Check out our list to see if your preferred currency is supported. Enjoy the convenience and flexibility of paying in your local currency!
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