The EU Qualified Person for Pharmacovigilance (EU QPPV) - Legal foundations, core responsibilities, and practical application

- Legal framework, liability, and legal protection - Regulatory requirements for day-to-day practice - Maintaining oversight of your pharmacovigilance system - Specific tasks, responsibilities, and possible delegations - Ensuring complianceThis two-day online course equips new, aspiring, and practising QPPVs with a clear understanding of their role under EU pharmacovigilance legislation, focusing on key responsibilities, strategic planning, and effective oversight. Learn what it takes to perform the role in practice while ensuring ongoing compliance.LernzieleThe Qualified Person for Pharmacovigilance (QPPV) holds a pivotal role for every Marketing Authorisation Holder (MAH) in the EU, carrying significant responsibility and a wide range of duties.- This course provides concise and practical guidance on the QPPVs responsibilities, grounded in the relevant legal framework. Upon completion, you will have a clear understanding of the expectations and regulatory obligations associated with this role, and you will be equipped to apply this knowledge confidently in your daily work. Real-life case studies, practical exercises, and interactive workshops will help you to successfully transfer what you have learnt into professional practice.ZielgruppenThis course will be conducted in English.- This course is designed for professionals with a basic understanding of pharmacovigilance who are aspiring to become (EU) QPPVs or serve as their deputies. It is also ideal for part-time QPPVs or anyone seeking a concise, high-impact refresher. While you do not need to be a QPPV to benefit from this course, a fundamental knowledge of pharmacovigilance is essential.