From Planning to Documentation
Webcode 25112051
Herta Anders
Wörwag Pharma GmbH & Co. KG, Boeblingen, ANDERS BERATEN, Weil der Stadt, GERMANY
Business Economist, Independent Project Manager and Coach;
Has been supporting numerous companies in the telecoms- and automotive industries as well as prospective and experienced managers and project managers since 2005. Since 2022 in the pharmaceutical industry at Wörwag as a consultant in project management and business coach.
More information please click here.
Reinhold Schilling
Wörwag Pharma GmbH & Co. KG, Böblingen, GERMANY
Head of Global Pharmacovigilance, EU-QPPV, local QPPV; Reinhold Schilling is a recognised expert in the field of pharmacovigilance, with more than a decade of experience in drug safety and regulatory affairs. After completing his degree in Chemistry at the University of Bonn and a part-time Master’s degree in Drug Regulatory Affairs, he specialised early in regulatory matters within the pharmaceutical industry. Since 2021, he has been serving as Head of Global Pharmacovigilance at Wörwag Pharma GmbH & Co. KG, where he leads the global drug safety department. In his role as EU Qualified Person for Pharmacovigilance (QPPV) and Stufenplanbeauftragter, he holds responsibility for ensuring compliance with international regulations, assessing medicinal product risks, and developing effective risk management strategies. In addition to his industry role, Reinhold is actively engaged in academia. He lectures on pharmacovigilance at Reutlingen University and Goethe Business School. Furthermore, as an active member of the BPI working group on pharmacovigilance, he contributes his expertise to the ongoing development of regulatory frameworks. His professional ambition is to continuously strengthen patient safety through clear processes, sound expertise, and strong leadership, with compliance serving as the cornerstone of all success.
11-13/11/2025
11-13/11/2025
Both days 09:00-17:00 CE(S)T
You may dial in 30 min before the session starts
online
online
Event - 2,090 € plus tax
The fee includes high-quality course materials (available for download), a certificate of participation, access to our Learning Space, and technical support, including a test meeting.
Event - 2,090 € plus tax
The fee includes high-quality course materials (available for download), a certificate of participation, access to our Learning Space, and technical support, including a test meeting.
Nadja Wolff
Conference Manager
+49 6221 500-696
n.wolff@forum-institut.de
- Newly designed and engagingly structured - This application-oriented online seminar is designed for pharmacovigilance professionals responsible for drug safety projects or those actively involved in project teams. Learn practical project management skills and benefit from discussing case studies in pharmacovigilance step by step.
This seminar combines comprehensive project management knowledge with the specific requirements of pharmacovigilance. During this two-day practice-oriented seminar, you will actively engage in workshops and case studies. Benefit from interactive collaboration using valuable templates that will help you streamline and optimise project execution within your organisation.
Our two experts from the fields of project management and pharmacovigilance will provide you with the essential tools to efficiently initiate, manage, monitor, and successfully complete PV projects. After attending, you will possess a comprehensive toolbox and practical techniques to manage projects effectively from within your PV department.
Do you have a specific project or questions in mind? Feel free to send them to us in advance at n.wolff@forum-institut.de - we will tailor the workshops to your individual needs!
After attending this online seminar, you will:
08:45 - 09:00
09:00 Welcome and introduction
09:15
Herta Anders
10:45 - 11:00 Coffee break
11:00
Reinhold Schilling
12:30 - 13:30 Lunch break
13:30
Herta Anders, Reinhold Schilling
15:15 - 15:30 Coffee break
15:30
Herta Anders, Reinhold Schilling
16:45 Key takeaways and questions
17:00 End of Day 1
09:00 Start of Day 2: Wrap-up of Day 1
09:15
Herta Anders, Reinhold Schilling
10:45 - 11:00 Coffee break
11:00
Herta Anders, Reinhold Schilling
12:30 - 13:30 Lunch break
13:30
Herta Anders, Reinhold Schilling
15:00 - 15:15 Coffee break
15:15
Herta Anders
16:45 Key takeaways and final discussion
17:00 End of course
Do you have a specific project or questions in mind? Feel free to send them to us in advance at n.wolff@forum-institut.de - we will tailor the workshops to your individual needs!
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 2024
of 5 stars on Trustpilot = good
Are you new to pharmacovigilance and looking to kick-start your career? Then this online course is just for you. Gain a ...
Do you want to independently plan and conduct pharmacovigilance audits? Then take this opportunity to become an "Auditor...
This online-seminar will provide tips on how to prepare and maintain a core PSMF as well as annexes with the relevant lo...
The Good Pharmacovigilance Practices modules (GVP modules) by the European Medicines Agency (EMA) serve as a reference f...
Join our interactive course to explore how AI is transforming pharmacovigilance. Take part in discussions, hands-on work...
