Dozent/in |
Dr. rer. pol. Dirk Lehnick |
Veranstaltungsart |
Masterseminar |
Code |
HS221310 |
Semester |
Herbstsemester 2022 |
Durchführender Fachbereich |
Gesundheitswissenschaften |
Studienstufe |
Master |
Termin/e |
Do, 06.10.2022, 14:15 - 16:00 Uhr, HS 14 Do, 13.10.2022, 14:15 - 16:00 Uhr, HS 14 Do, 20.10.2022, 14:15 - 16:00 Uhr, ZOOM Do, 27.10.2022, 14:15 - 16:00 Uhr, HS 14 Do, 03.11.2022, 14:15 - 16:00 Uhr, HS 14 Do, 10.11.2022, 14:15 - 16:00 Uhr, HS 14 Do, 17.11.2022, 14:15 - 16:00 Uhr, HS 14 Do, 24.11.2022, 14:15 - 16:00 Uhr, HS 14 Do, 01.12.2022, 14:15 - 16:00 Uhr, HS 14 Do, 15.12.2022, 14:15 - 16:00 Uhr, HS 14 Do, 22.12.2022, 14:15 - 16:00 Uhr, ZOOM Do, 19.01.2023, 08:30 - 10:00 Uhr, 3.B58 (Prüfung) |
Weitere Daten |
Mandatory Basic Course for MSc Health Sciences students which started in fall 2021. |
Umfang |
2 Semesterwochenstunden |
Inhalt |
Clinical Trials:
• Interventional vs. non-interventional studies • Trials involving medicinal products / Phases of drug development • Study objectives • Typical study designs • Randomization, blinding, study documentation, sample size determination
Good Clinical Practice (GCP) and Research Ethics:
• Ethical principles for research • History of clinical research ethics (incl. case studies) • Good Clinical Practice guidelines / legal framework • Roles, tasks and responsibilities in clinical studies as defined by ICH-GCP • Patient information and consent • Clinical trial application / Ethics committees / Competent authorities • Scientific requirements and practical implementation issues • Quality management in clinical trials • Patient information and consent • Data collection and handling / Statistical planning and analysis • Adverse events and safety reporting
|
Lernziele |
• Gain basic knowledge of principles of clinical trials
• Understand the historical context and main concepts of research ethics and Good Clinical Practice (GCP) guidelines
• Know roles, tasks and responsibilities in clinical studies as defined by ICH-GCP |
Voraussetzungen |
Diligence and eagerness to learn. |
Sprache |
Englisch |
Begrenzung |
priority Master Health Sciences students |
Anmeldung |
https://elearning.hsm-unilu.ch/course/view.php?id=570 |
Prüfung |
The course credits will be earned by passing a written exam in at the end of the semester or, in case of failure of the written test, the passing of a compensation test during the subsequent semester. |
Abschlussform / Credits |
written exam / 3 Credits
|
Hinweise |
Teaching method(s):
The module mainly consists of in-class teaching complemented by practical learning sessions and problem discussions. In-class teaching sessions will be electronically available for recapitulation. Parts of the course will be require self-study conducted between in-class lectures based upon case studies and documents which will be electronically available or will be handed out during the sessions. |
Hörer-/innen |
Nein |
Kontakt |
dirk.lehnick@unilu.ch |
Material |
All teaching material incl. case studies will be provided via the learning management system or as handout. |
Literatur |
Swiss Academy of Medical Sciences (SAMS) handbook “Research with human subjects” (2nd edition, 2015) Emanuel et al. (2000) What makes clinical research ethical; JAMA 283(20):2701-2711 ICH GCP Guideline with Integrated Addendum E6(R2), Step 4 (Nov 2016)
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