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Free Download Master Pharmacovigilance From A To Z. Get Certified
Published 11/2025
MP4 | Video: h264, 1920x1080 | Audio: AAC, 44.1 KHz
Language: English | Size: 11.72 GB | Duration: 10h 48m
Mastering Pharmacovigilance: From Basics to Advanced Drug Safety Practices, and AI, your full review of all topics of PV
What you'll learn
Understand the core principles and objectives of pharmacovigilance and its critical role in ensuring drug safety.
Identify and describe the types, sources, and classifications of adverse drug reactions (ADRs) and adverse events (AEs).
Navigate global pharmacovigilance regulations and guidelines - including those from the FDA, EMA, WHO, MHRA, and ICH.
Explain the end-to-end process of case processing, including data collection, coding, assessment, and reporting.
Apply risk management principles and create Risk Management Plans (RMPs) and Periodic Safety Update Reports (PSURs/PBRERs).
Recognize signal detection methods and understand how safety signals are evaluated and managed.
Use pharmacovigilance databases and systems such as EudraVigilance, FAERS, and VigiBase for safety reporting.
Communicate effectively with regulatory authorities and stakeholders to ensure compliance and transparency.
Analyze real-world case studies to understand how pharmacovigilance impacts regulatory decisions and patient safety.
Develop a career roadmap in pharmacovigilance and understand the competencies required for various PV roles.
Requirements
A basic understanding of life sciences, pharmacy, medicine, or healthcare concepts.
Familiarity with clinical research or regulatory affairs terminology (helpful but not mandatory).
Curiosity about how medicines are monitored for safety, quality, and compliance after approval.
Motivation to build or advance a career in the pharmaceutical, biotech, or healthcare industry.
Access to a computer or tablet with internet connection to explore regulatory databases, tools, and course resources.
Description
The Pharma Academy! Alwyas comes to you from prcatice ! and Updates! You are ete next QPPV/LSR !You are the next PV Auditor !Are you ready to take your career in pharmaceuticals and healthcare to the next level? Pharmacovigilance (PV) is the cornerstone of drug safety, ensuring that medications are not only effective but safe for patients worldwide. This comprehensive course is designed for professionals, students, and anyone passionate about drug safety, offering both foundational knowledge and practical, industry-ready skills.In this course, you will:Understand the Essentials: Learn the key principles of pharmacovigilance, drug safety regulations, and the global framework that governs adverse event reporting.Master Real-World PV Processes: Gain hands-on knowledge in signal detection, risk management, case processing, and regulatory submissions.Navigate Regulatory Landscapes: Explore the latest requirements in the FDA, EMA, ICH, and other global health authorities.Boost Your Career: Acquire the skills that top pharmaceutical companies and CROs are seeking in PV specialists, drug safety officers, and regulatory affairs professionals.Topics you will master?Definition of the PV The need for the PV The PV History The Emergance of the PV in the Pharma industry Structure of the PV PV process ICSR Case Managmnet CASESPSMF/PSSFCommon Arab Guidleines for PV PSUR PV AuditPV Signals PV PASSPV RMP PV Communication PV CAPA PVImpact PV Tracking and Tracing AI Closing Why this course is different
ractical, real-world examples from the pharmaceutical industryStep-by-step guidance on navigating complex PV databases and reporting systemsInsights into global regulatory updates that impact your daily workEngaging content designed for fast comprehension, even if you are new to PVBy the end of this course, you'll be confident in your ability to handle pharmacovigilance tasks with accuracy and professionalism, making you a valuable asset in any healthcare or pharmaceutical setting.Enroll now and start your journey to becoming a skilled pharmacovigilance professional - because patient safety isn't just a requirement, it's a responsibility.Pharmacy, medical, and life science graduates who want to build a strong foundation and start a rewarding career in pharmacovigilance or drug safety.,Regulatory affairs, clinical research, and medical affairs professionals seeking to expand their expertise in post-marketing safety and compliance.,Healthcare professionals - including doctors, nurses, and pharmacists - who want to understand how adverse events are reported, assessed, and managed.,Pharmaceutical and biotech industry employees who wish to enhance their understanding of global PV systems and regulatory requirements.,Job seekers and career changers exploring new opportunities in pharmacovigilance, drug safety, or clinical data management.,Students and early-career professionals looking for practical, step-by-step guidance to enter one of the fastest-growing fields in healthcare.
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