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Key Objectives of GVP: Early detection of safety signals Continuous benefitrisk evaluation Timely reporting of adverse events Regulatory compliance Protection of patient health Core GVP Modules Include: GVP Module I Pharmacovigilance Systems & Quality Management Module II Pharmacovigilance System Master File (PSMF) Module VI Management & Reporting of Adverse Reactions Module VII Periodic Safety Update Reports (PSUR/PBRER) Module VIII Post-Authorization Safety Studies (PASS) Module IX Signal Management Module X Additional Monitoring Why GVP Matters for PV Professionals: Adhering to GVP ensures regulatory readiness, audit preparedness, and most importantly-patient safety

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