Angela Hartmann
Senior Expert Pharmacovigilance, Darmstadt, GERMANY
Audit, Inspection, Deviation and CAPA Manager Ms Hartmann has many years of experience in drug safety in international pharmaceutical companies, including case handling, process management, pharmacovigilance database management, global literature research, clinical trials, audits and inspections.
Per-Holger Sanden
Merck Healthcare KGaA, Darmstadt, GERMANY
Inspection Management Lead Per-Holger Sanden is an experienced and dedicated physician with extensive expertise in pharmaceutical quality assurance and process optimisation. He has been Head of Inspection Management at Merck Healthcare KGaA for almost eight years, where he coordinates over 160 inspection teams worldwide in the areas of GCP, GVP and GLP. A pragmatic troubleshooter and adept mediator, he brings not only his extensive expertise but also his passion for quality risk management and computer system validation.
Dr. Kimberley Sherwood
Senior Expert Pharmacovigilance, Bonn
Senior Expert Pharmacovigilance
24/03/2025
24/03/2025
09:00-17:30 CET
You may dial in 30 min before the session
online
online
Event - 1,290 € 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 - 1,290 € 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
Learn how to prepare your pharmacovigilance system in Germany, Europe and worldwide for an upcoming inspection in this one-day online course. Gain a comprehensive understanding of the EMA's Good Pharmacovigilance Practice (GVP/GPvP) modules, strategic and remote planning and preparation, and differences in GVP inspections around the world. Reserve your seat in our virtual seminar room.
To ensure that marketing authorisation holders comply with their pharmacovigilance obligations, competent authorities conduct pharmacovigilance inspections at specified intervals. This online course provides an insight into current (remote) pharmacovigilance inspection strategies.
After attending this online seminar you will be able to...
This seminar will equip you to prepare for pharmacovigilance inspections professionally, adhering to legal requirements and best practices.
Engage with experts from authorities and industry to discuss your questions and find the answers you need.
After the seminar, you will gain a thorough understanding of current pharmacovigilance inspection strategies and be able to enhance your processes in Germany, Europe and worldwide.
08:45
09:00
FORUM Institut
09:15
Dr Kimberley Sherwood
09:45
Per-Holger Sanden
10:45 Coffee break
11:00
Per-Holger Sanden
11:45
Per-Holger Sanden, Angela Hartmann
12:15 Lunch break
13:00
Per-Holger Sanden, Angela Hartmann
13:30
Dr Kimberley Sherwood
14:30
Per-Holger Sanden, Angela Hartmann
15:45 Coffee break
16:00
Angela Hartmann
16:30
All speakers
17:15
17:30 Seminar ends
Are you ready to challenge your pharmacovigilance knowledge? Our interactive quiz offers an engaging and enjoyable way to assess your expertise.
Simply click on the answers you think are correct!
You need a reliable Internet connection to take part in our online events. To have the best possible learning experience, we recommend that you use the latest version of the Microsoft Edge or Google Chrome browsers. You will need a headset, loudspeaker or telephone to play the audio. Further information is available here. Please check beforehand that your microphone or headset and camera are working properly. Do not access our services from a VPN since there are issues with the audio over such connections.
We have integrated Zoom video conferencing software into our Learning Space for our online training courses. If you are not authorised to use Zoom, please get in touch with us so we can make alternative arrangements for you to take part in our online training.
Once you have registered for an event, we will send you the access information for your customer portal. Click here to log in to the customer portal using your email address and password. Please ensure you can access the customer portal before the day of the event.
All important or additional information and personal documents are available in your personalised customer portal. This is also where you start your online courses. If you do not have access to the customer portal yet, you can easily register here.
On the day of the event, you kick off your online training in the customer portal by clicking ‘Participate’ directly in the respective event. You will then be redirected to the Learning Space.
Learn more about our online events here.
of 5 stars of all ratings from 2023
of 5 stars on Trustpilot = good
Reporting adverse drug reactions forms the foundation of drug safety. In this one-day online seminar, you will learn the...
This online seminar provides a comprehensive overview of global regulatory affairs, covering strategies for setting regu...
Update your knowledge: Our team of experts provides you with important and practical information about the tasks and res...
This online-seminar will provide tips on how to prepare and maintain a core PSMF as well as annexes with the relevant lo...
Our global and local experts will update you every two months with the latest regulatory and legislative developments. T...
All speakers provided excellent content and explanation of the content.
Very useful to get an overview of the procedure.
Good & clear training in pharmacovigilance inspection readiness. Clear and very good speakers.
Bita Mangin
Sanofi Aventis Groupe, Paris
Practical examples related to PV inspection requests.
Sharing of examples from recent experiences.
Possibility to hear from other companies about their inspection experiences.