Starter and refresher of the duties and responsibilities of a QPPV
Webcode 24022052
Dr. Christian M. Moers
Sträter Lawyers, Bonn, GERMANY
Lawyer;
His prime interests are the interdisciplinary challenges of medicinal product law. His focal advisory areas are as follows:
- European and German medicinal product law
- Marketing authorisation law & regulatory affairs
- Pharmacovigilance
- Wholesale trade with medicinal products, distribution of medicinal products
- Manufacture of medicinal products
More information please click here.
Reinhold Schilling
Wörwag Pharma GmbH & Co. KG, Boeblingen, GERMANY
Head of Global Pharmacovigilance, EU-QPPV
21/02/2024
21/02/2024
09:00 - 17:00You may dial in 30 min....
09:00 - 17:00
You may dial in 30 min. before the session.
online
online
Event - 1,190 € plus tax
The fee includes high-quality course material for download, a participation certificate, access to the Learning Space as well as technical support including a test meeting.
Event - 1,190 € plus tax
The fee includes high-quality course material for download, a participation certificate, access to the Learning Space as well as technical support including a test meeting.
Nadja Wolff
Conference Manager
+49 6221 500-696
n.wolff@forum-institut.de
Update your knowledge: Our team of experts provides you with important and practical information about the tasks and responsibilities of an EU-QPPV.
The Qualified Person for Pharmacovigilance (QPPV) is a central role in any pharmaceutical company, with a high level of responsibility and a variety of duties.
This course provides critical and practical information about the duties of a QPPV and the legal basis for their activities.
It will also examine the major issue of liability and discuss the consequences of Brexit for an EU QPPV.
This course will familiarise you with the roles, responsibilities and liabilities of a QPPV in the EU and explain how to integrate pharmacovigilance in your company.
It will also focus on how a QPPV delegates tasks, and provide useful tips on how to build a worldwide QPPV network.
09:00
09:20
Dr Christian M. Moers
10:05 Coffee break
10:20
Reinhold Schilling
11:30
Reinhold Schilling
12:40 Lunch break
13:30
Reinhold Schilling
14:15
Reinhold Schilling
15:15 Coffee Break
15:30
Dr Christian M. Moers
16:45 Discussions and/or Q&A session
17:00 End of course
Overall impression: 100% of the participants’ feedback was very good or good (February 2023)
Seminar content: 100% of the participants’ feedback was very good or good (February 2023)
This online-seminar will provide tips on how to prepare and maintain a core PSMF as well as annexes with the relevant lo...
During this winter school you will build a solid toxicological know-how basis and will be informed about the inclusion o...
Our global and local experts will update you every two months with the latest regulatory and legislative developments. T...
This course familiarises you with regulatory post-approval duties and provides first-hand information on variation submi...
Learn the essentials of the MDR and how to navigate around the legislation and to apply it.
