Dr. Grit Lynch
Biotest AG, Dreieich,
Director CDS Operations, Corporate Drug Safety
Claudia Schaffer
Merck Healthcare KGaA, Darmstadt
Sr. Director, Head Case and Vendor Management Biopharma - Global Patient Safety - Operations
10/03/2025
10/03/2025
09:00-17:00 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
Reporting adverse drug reactions forms the foundation of drug safety. In this one-day online seminar, you will learn the regulatory requirements and best practices for ICSR reporting. Whether you are new to the topic or looking for a refresher, you will benefit from the extensive practical experience of our speakers from both Big Pharma and consulting!
This seminar aims to provide participants with comprehensive knowledge of Individual Case Safety Reporting (ICSRs) according to the guidelines of GVP Module VI. You can expect the following:
After the seminar, you will:
Dr Grit Lynch
Coffee break
Dr Grit Lynch
Lunch break
Claudia Schaffer
Claudia Schaffer
Coffee break
Claudia Schaffer, Dr Grit Lynch
Dr Grit Lynch, Claudia Schaffer
End of Seminar
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