The one-day course in Pharmacovigilance provides an overview of drug safety and the monitoring of adverse drug reactions. Participants will learn key concepts, regulatory frameworks, and best practices in pharmacovigilance. The course covers methodologies for reporting, risk assessment, and the importance of post-marketing surveillance in ensuring patient safety. Ideal for healthcare professionals and those in the pharmaceutical industry, this course aims to enhance understanding of the critical role of pharmacovigilance in public health.
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Requirements
- Pharmacists and healthcare professionals involved in patient care. - Regulatory affairs specialists and quality assurance personnel. - Clinical research associates and professionals in the pharmaceutical industry. - Anyone interested in enhancing their knowledge of drug safety and pharmacovigilance practices
Outcomes
By the end of the course, participants will be able to: - Understand the role of pharmacovigilance in ensuring drug safety. - Identify and report adverse drug reactions effectively. - Assess and manage risks associated with pharmaceutical products. - Navigate regulatory requirements and contribute to compliance efforts within their organizations.
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