QPPV and LCPPV: Evolution of Pharmacovigilance Roles
History of QPPV and LCPPV: Evolution of Pharmacovigilance Roles Qualified Person for Pharmacovigilance (QPPV) and Local Contact Person for Pharmacovigilance (LCPPV) are pivotal roles in
Medical Device Pharmacovigilance
Medical Device Pharmacovigilance: Ensuring Safety in the Era of Technological Advancements In the dynamic field of healthcare, medical devices have become indispensable tools, complementing or
Types of Pharmacovigilance: A Comprehensive Overview
Types of Pharmacovigilance encompass various approaches to monitoring the safety and efficacy of medicinal products throughout their lifecycle. These methods ensure that potential risks associated
QPPV Requirements in Asian countries
The Qualified Person for Pharmacovigilance (QPPV) is a critical role in ensuring the safety and monitoring of pharmaceutical products in many countries, including those in
Checklists for Compliance with Pharmacovigilance Regulations
IntroductionCompliance with pharmacovigilance (PV) regulations is a cornerstone of ensuring drug safety and maintaining trust with regulatory authorities. This expanded checklist provides detailed, actionable steps
Pharmacovigilance Courses
Understanding Pharmacovigilance Courses: A Gateway to Drug Safety and Public Health Pursuing a pharmacovigilance courses is an excellent way for healthcare professionals, scientists, and aspiring
The World Drug Safety Congress
The World Drug Safety Congress: A Platform for Advancing Pharmacovigilance and Drug Safety The World Drug Safety Congress (WDSC) is a globally recognized event that
Semaglutide Safety: A Scientific Overview
Semaglutide, a GLP-1 receptor agonist, has shown significant efficacy in managing type 2 diabetes, obesity, and associated cardiovascular risks. However, Semaglutide safety profile necessitates careful
Active Pharmacovigilance: Enhancing Drug Safety Monitoring
Introduction Pharmacovigilance plays a pivotal role in safeguarding public health by monitoring the medicines safety. While passive pharmacovigilance relies on voluntary reporting of adverse drug