Prof. Dr. Michael Arand
Institute of Pharmacology and Toxicology, University of Zurich, SWITZERLAND
Professor in the Institute for Pharmacology and Toxicology
Dr. Bernd-Bodo Haas
Expert for Toxicology, Bonn
Specialist in Genetic and Reproductive Toxicology He works at the Genetic and Reproductive Toxicology, Bundesinstitut für Arzneimittel und Medizinprodukte and does research in Diabetology, Pharmacy and Toxicology.
Dr. Hans-Joerg Martus
Novartis Institutes for BioMedical Research (NIBR), Basel, SWITZERLAND
Head of Genome Safety and Project Toxicologist
Dr. Niklas Czeloth
Boehringer Ingelheim Pharma GmbH & Co. KG, Ingelheim, GERMANY
He is an Investment Manager in the Boehringer Ingelheim Venture Fund with 15 years of experience in pharmaceutical development.
Dr. Anika Schröter
Dr. Anika Schroeter e.U., Vienna, AUSTRIA
Anika Schröter holds a PhD in toxicology and is a registered European Registered Toxicologist. Since 2014 she has been working as a consultant for clients in the pharmaceutical and biotech industry on issues related to non-clinical drug development (e.g. small molecules, biologics, vaccines). Her expertise includes the creation of non-clinical development programs, design and supervision of GLP toxicology studies, or support in consultations with European or non-European authorities. Since 2021 she runs her own consulting company in Vienna.
17-18/02/2025
17-18/02/2025
Both days II: 9:00 am - 5:00 pm - seminar
You may dial in 30 minutes before the training starts
online
online
Event - 1,990 € plus tax
The participation fee includes documentation for download, a certificate, access to the Learning Space and technical support including PreMeeting.
Event - 1,990 € plus tax
The participation fee includes documentation for download, a certificate, access to the Learning Space and technical support including PreMeeting.
Dr. Birgit Wessels
Conference Manager
+49 6221 500-652
b.wessels@forum-institut.de
During our online training "Toxicology and beyond: Safety assessment in drug development" you will build a solid toxicological know-how basis and will be informed about the inclusion of toxicological data in the marketing authorisation dossier. Take the chance and participate in our interactive online training.
09:00 Welcome, expectations, introduction
09:15
Prof Dr Michael Arand
10:15 Coffee break
10:30
Prof Dr Michael Arand
11:45 Lunch break
12:45
Dr Bernd-Bodo Haas
15:30
Dr Bernd-Bodo Haas
16:15
Dr Bernd-Bodo Haas
17:00 Q&As and end of training day 1
09:00
Dr Hans-Joerg Martus
10:30 Coffee break
10:45
Dr Hans-Joerg Martus
11:45
Dr Hans-Joerg Martus
12:30 Lunch break
13:30
Dr Niklas Czeloth
15:00 Coffee break
15:15
Dr Anika Schröter
16:45 Q&As
17:00 End of training day 2
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