Course description

Medicines have revolutionized healthcare, but their use is not without risks. Adverse drug reactions (ADRs) contribute significantly to patient morbidity and mortality worldwide. To ensure the safe and effective use of medicines, healthcare professionals, regulators, and pharmaceutical experts must be well-versed in pharmacovigilance.

This comprehensive course provides an in-depth understanding of pharmacovigilance, covering topics such as ADR detection, risk assessment, drug safety regulations, signal detection, and regulatory reporting frameworks (e.g., WHO, FDA, EMA). Participants will explore real-world case studies and gain practical skills in adverse event monitoring, benefit-risk assessment, and post-marketing surveillance.

Designed for healthcare professionals, pharmacists, regulators, researchers, and industry stakeholders, this course empowers learners with the knowledge and tools to enhance medication safety and protect public health on a global scale. Whether you are new to the field or seeking to expand your expertise, this course offers a valuable foundation in pharmacovigilance.

What will i learn?

• Understand the principles and importance of pharmacovigilance in ensuring drug safety
• Identify and assess adverse drug reactions (ADRs) and drug-related risks
• Apply regulatory frameworks and guidelines (FDA, EMA, WHO) in pharmacovigilance practices
• Conduct post-marketing surveillance and signal detection to improve medication safety
• Develop risk mitigation strategies and safety reporting mechanisms
• Enhance professional competency in drug safety roles within healthcare and pharmaceutical industries

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