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28942-01 - Vorlesung: Animal Experimentation for Regulatory Purposes 2 KP

Semester Herbstsemester 2022
Angebotsmuster Jedes Herbstsemester
Dozierende Mark Deurinck (mark.deurinck@unibas.ch, BeurteilerIn)
Inhalt Why do we perform animal experiments? How do we perform them? Who is regulating theme? Are we working on alternative tests? We will be discussing the principles, regulations and ethics of non-clinical studies, study design and endpoints, interpretation and application of results, in drug development.
Lecturers will be joining us from industry and academia, on a much appreciated voluntary basis.

Program overview (chronological order may vary):
- Animal Experimentation for Regulatory Purposes: Introduction to the module
- Species-specific Effects in Toxicity: Understanding and extrapolation to humans
- Regulatory toxicology: Health hazard assessment of drugs in the frame of regulations
- Toxicology: Study types, dose, species, study duration; basic study protocol; technologies
- Safety Pharmacology: Cardiovascular endpoints and models used in drug development
- Haematology, Clinical Chemistry, Urinalysis: Basic principles
- Mode of action and biological targets: pharmacology and toxicology; human extrapolation
- In silico tools for development of biologics
- Regulatory Toxicology for pharmaceutical intermediates
- Reproductive Toxicology: Studies and interpretation of results for human risk assessment
- Ethics in Animal Experimentation and legal requirements
- Carcinogenicity studies and in vivo genotoxicity
- Risk assessment for patient safety in manufacturing, incl. case study
Lernziele Understand scientific and regulatory background of preclinical animal studies conducted during development and registration of drugs and chemicals and the interpretation of data for human health risk assessment.
Literatur Provided during the lecture period
Bemerkungen Film and sound recordings during the course are strictly forbidden (recorders may be confiscated)
Weblink Department of Pharmaceutical Sciences

 

Teilnahmebedingungen Completed Bachelor degree
Anmeldung zur Lehrveranstaltung
Unterrichtssprache Englisch
Einsatz digitaler Medien kein spezifischer Einsatz

 

Intervall Wochentag Zeit Raum
wöchentlich Mittwoch 15.15-17.00 Biozentrum, Seminarraum U1.191

Einzeltermine

Datum Zeit Raum
Mittwoch 21.09.2022 15.15-17.00 Uhr Biozentrum, Seminarraum U1.191
Mittwoch 28.09.2022 15.15-17.00 Uhr Biozentrum, Seminarraum U1.191
Mittwoch 05.10.2022 15.15-17.00 Uhr Biozentrum, Seminarraum U1.191
Mittwoch 12.10.2022 15.15-17.00 Uhr Biozentrum, Seminarraum U1.191
Mittwoch 19.10.2022 15.15-17.00 Uhr Biozentrum, Seminarraum U1.191
Mittwoch 26.10.2022 15.15-17.00 Uhr Biozentrum, Seminarraum U1.191
Mittwoch 02.11.2022 15.15-17.00 Uhr Pharmazentrum, Examination weeks
Mittwoch 09.11.2022 15.15-17.00 Uhr Biozentrum, Seminarraum U1.191
Mittwoch 16.11.2022 15.15-17.00 Uhr Biozentrum, Seminarraum U1.191
Mittwoch 23.11.2022 15.15-17.00 Uhr Biozentrum, Seminarraum U1.191
Mittwoch 30.11.2022 15.15-17.00 Uhr Biozentrum, Seminarraum U1.191
Mittwoch 07.12.2022 15.15-17.00 Uhr Biozentrum, Seminarraum U1.191
Mittwoch 14.12.2022 15.15-17.00 Uhr Biozentrum, Seminarraum U1.191
Mittwoch 21.12.2022 15.15-17.00 Uhr Pharmazentrum, Examination weeks
Module Modul: Translating Pharmacology and Drug Safety to Humans (Masterstudium: Drug Sciences)
Wahlbereich Master Pharmazie: Empfehlungen (Masterstudium: Pharmazie)
Leistungsüberprüfung Lehrveranst.-begleitend
Hinweise zur Leistungsüberprüfung Written examination at the end of the semester (multiple Choice, possibly some essay questions)
https://pharma.unibas.ch/en/education/assessments-and-credit-points/continuous-assessments/
An-/Abmeldung zur Leistungsüberprüfung Anm.: Belegen Lehrveranstaltung; Abm.: stornieren
Wiederholungsprüfung keine Wiederholungsprüfung
Skala 1-6 0,5
Wiederholtes Belegen beliebig wiederholbar
Zuständige Fakultät Philosophisch-Naturwissenschaftliche Fakultät, studiendekanat-philnat@unibas.ch
Anbietende Organisationseinheit Departement Pharmazeutische Wissenschaften

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