FORUM INSTITUT
FORUM · Institut für Management GmbH
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Seminare zu Clinical & medical affairs
Toxicology
Winter School
2017-12-23 2018-01-25 Mercure Hotel Mannheim am Rathaus F7,5 68159 Mannheim H5410-SB@accor.com +49 621 336990 +49 621 33699-2100

Toxicology Winter School

Know-how for employees in R&D, medical affairs, regulatory affairs and pharmacovigilance

During this Winter School you will build a solid toxicological know-how basis and will be informed about the inclusion of toxicological data in the marketing authorisation dossier.
Topics
  • Toxicokinetics and drug-drug interaction
  • Mutagenicity and genotoxicity
  • Carcinogenicity
  • Reproductive toxicity and safety pharmacology
  • Immunogenicity
  • Ecotoxicity and environmental risk assessment

This distinguishes our event

100%
Overall impression: 100 % of the participants' feedback was very good or good (January 2017)
100%
Course content: 100 % of the participants' feedback was very good or good (January 2017)
100%
Practical benefit: 100 % of the participants' feedback was very good or good (January 2017)

Aims and objectives

During this winter school:

  • you will build a solid toxicological know-how basis;
  • you will get to know the essential toxicological modes of action and learn how to apply them to your products;
  • you will receive good insights into the toxicological study programme and learn how it must be scheduled in drug development;
  • you will be informed about the inclusion of toxicological data in the marketing authorisation dossier and the associated regulatory affairs duties.

Who should attend?
This winter school addresses the need for solid toxicological know-how of employees in the pharmaceutical industry, particularly those in the following departments:

  • Research and development
  • Medical affairs
  • Regulatory affairs
  • Pharmacovigilance

Basic scientific/medical knowledge would be helpful, toxicological know-how is not expected.
Your speakers
Prof. Dr. Michael Arand
University of Zurich, SWITZERLAND

Dr. Susanne Brendler-Schwaab
Senior Expert Regulatory Affairs, Bonn, GERMANY

Dr. Monika Chabicovsky
MC Toxicology Consulting GmbH, Vienna, AUSTRIA

Dr. Niklas Czeloth
Boehringer Ingelheim Pharma GmbH & Co. KG, Ingelheim, GERMANY

Hans-Joerg Martus, PhD
Preclinical Safety (PCS), Novartis Institutes for BioMedical Research (NIBR), Basel, SWITZERLAND


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More on our quality criteria

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IMI (Innovative Medicines Initiative) defined quality criteria for professional training and education. We follow these criteria and, as a signatory, we are an active partner in further developing and optimising the quality standards.

An aggregate evaluation of participants' feedback on all FORUM's healthcare training courses (evaluation period from 10.2015 - 09.2016 produced a result of 1.7 (based on a school grading system of 1-6).

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