Certificate in EU Pharmacovigilance Guidelines Overview
-- ViewingNowThe Certificate in EU Pharmacovigilance Guidelines Overview is a comprehensive course that provides learners with an in-depth understanding of the European Union's pharmacovigilance guidelines. This course is essential for professionals working in the pharmaceutical industry, as it covers the critical aspects of drug safety and risk management in the EU.
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โข Introduction to Pharmacovigilance
โข EU Pharmacovigilance Guidelines: Overview and Importance
โข The Role of the European Medicines Agency (EMA) in Pharmacovigilance
โข Key Components of EU Pharmacovigilance Legislation
โข EU Pharmacovigilance System Master File (PSMF) Requirements
โข Pharmacovigilance Risk Assessment Committee (PRAC) and its Responsibilities
โข Adverse Drug Reaction (ADR) Reporting in the EU
โข Periodic Safety Update Reports (PSURs) and their Significance
โข EU Database of Adverse Drug Reactions (EADR): Access and Utilization
โข Inspections and Enforcement in EU Pharmacovigilance
โข Continuous Pharmacovigilance Training and Education
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