Course description

This course provides a comprehensive foundation in science and activities relating to the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems, forming a critical component of patient safety and public health. Participants will learn the global regulatory framework governing pharmacovigilance, master the processes for adverse event reporting and management, and develop skills in risk assessment, signal detection, and the development of risk minimization strategies. By understanding the entire pharmacovigilance lifecycle, from clinical trials to post-marketing surveillance, you will be equipped to ensure the ongoing safety of pharmaceutical products and contribute to the safe and effective use of medicines for patients worldwide.

What will i learn?

Requirements

4.0

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5.0
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4.0
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3.0
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2.0
129 reviews
1.0
217 reviews

Free

Lectures

0

Skill level

Beginner

Expiry period

Lifetime

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