Safety Pharmacology (Safety Pharmacology)
Owner/Developer: Helmholtz Zentrum München & German Society for Experimental and Clinical Pharmacology and Toxicology (HMGU & DGPT)
| Country: |
Germany |
|---|---|
| Url: |
https://www.helmholtz-muenchen.de/toxkurse/kurse/kursuebersicht/safety-pharmacology/index.html |
| Created: |
01 January 0001 |
| Locations: |
Switzerland |
| City: |
Basel |
| Description: |
In 1979, the then existing toxicology section of the German Society for Experimental and Clinical Pharmacology and Toxicology launched its DGPT toxicology qualification program to promote the education and training of young people in toxicology. It offers theoretical training in all areas of the discipline of toxicology.
The aim of the program is to impart skills and knowledge according to DGPT toxicology training guidelines. The course in Safety Pharmacology is part of the toxicology program at HMGU. This course is intended to provide a unique overview of an important discipline in pharmaceutical industry. The participant will have an understanding of the various test systems used and the integration of Safety Pharmacology in the drug development process. |
| References: |
https://www.helmholtz-muenchen.de/en/career/further-training/toxicologist-dgpt/index.html |
| Format: |
Hands-on training, Lecture |
| Presence: |
Mandatory |
| Access: |
Fee-based |
| Content type: |
Theoretical, Practical |
| Frequency: |
Recurrent event |
| Target audience: |
Students, Researchers |
| Target sectors: |
Academia, Industry |
| Educational level: |
Continuing Professional Development |
| 3rs relevance: |
Refinement, Reduction, Replacement |
| Topics covered: |
Carrying out procedures on animals, Computational methods, In vitro methods |
| 3rs coverage: |
Partial coverage (e.g. a module) |
| Species covered: |
No species is addressed specifically |
| Course level on animal species: |
Advanced course |
| Details on the topic or technology covered: |
Introduction into Safety Pharmacology, regulatory, guideline and good-laboratory-practice (GLP) background.
Cardiovascular basics, in-silico, in-vivo, and in-vitro models, evaluation of ECGs and introduction into cardiac arrhythmias. CNS basics, core battery and supplemental studies, concordance with clinics. Anatomy and physiology of respiration, tests on respiration. Pharmacokinetics, Modeling and Simulation. Basics on statistics. Renal function, metabonomics and gastrointestinal function. Oncologics and biologics. Integrated risk assessment. Human ECG studies, translational medicine. Practical part in groups (cardiovascular telemetry labs, CNS labs, respiration labs). |
| Learning outcome: |
Understanding of the various test systems used and the integration of Safety Pharmacology in the drug development process. |
| Accreditation body and/or authority that approved the education or training: |
DGPT |
| Qualification received: |
Expert in Toxicology, DGPT |
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