Gain a comprehensive understanding of the pivotal role of the Qualified Person Responsible for Pharmacovigilance (QPPV) with our engaging course, “Introduction to the Role of QPPV.” Whether you’re new to pharmacovigilance or seeking to deepen your expertise, this course offers essential insights into the legal framework, regulatory requirements, and key responsibilities associated with the QPPV role.
As a central figure in the pharmacovigilance system, the QPPV plays a crucial role in ensuring the safety and effectiveness of medicinal products. Through this course, you’ll explore:
- Basic abbreviations, terminology, and key concepts related to the QPPV role.
- Regulatory requirements and guidelines governing pharmacovigilance in the EU.
- Roles and responsibilities of the EU QPPV, including oversight of the pharmacovigilance system and specific medicinal products.
- Preparation strategies for inspections and audits as a QPPV, along with an overview of PV inspection types.
- Supervision of the pharmacovigilance system in both small pharmaceutical companies and global corporations.
- Configuration of a complete PV system, including task delegation processes, PSMF oversight, and quality management.
- Management of service providers, business partners, and product safety issues, including signal and risk management.
Course Highlights:
- Expertly crafted presentation to provide in-depth insights into the role of the QPPV.
- Obtain a recognized certificate upon successfully passing the course test.
- Collaborate and discuss course content with fellow learners on the AIDIFY platform, enhancing your understanding through interaction.
Would you like to know more? Join the course!
