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45395-01 - Lecture: Good Clinical Practice (1 CP)
| Semester | fall semester 2026 |
| Course frequency | Every fall sem. |
| Lecturers |
Eric Huber (eric.huber@unibas.ch, Assessor)
Elisabeth Anne Reus (elisabeth.reus@unibas.ch) Meera Saxena (meera.saxena@unibas.ch) |
| Content | Compact two day introductory course to the Good Clinical Practice guideline (GCP) designed according to the requirements of Swissethics. The course provides a compact insight into the ICH E6 GCP regulation and related topics. It is ideal for Investigators, study personnel and people involved and/or interested in clinical research. Content: Principles of the ICH-GCP guideline and its historical background; Study design and basic statistical principles; Legal and regulatory requirements of clinical research; Essential study documentation, incl. structure and content of study protocol; An overview of how data is processed in clinical trials: Informed consent and safety aspects; Quality and data management in clinical trials; Ethics and submission processes (in Switzerland) |
| Learning objectives | Understanding the basic principles of research involving humans Knowing the fundamental principles of Good Clinical Practice |
| Bibliography | Mandatory reading: Declaration of Helsinki - Ethical Principles for Medical Research Involving Human Subjects Version 2012 https://www.wma.net/policies-post/wma-declaration-of-helsinki-ethical-principles-for-medical-research-involving-human-subjects/ -> detailed pre-reading required Guideline ICH E8(R1) General considerations for clinical studies https://www.ema.europa.eu/en/ich-e8-general-considerations-clinical-studies-scientific-guideline - detailed pre-reading required Guideline ICH E6(R3) Good Clinical Practice https://www.ich.org/page/efficacy-guidelines - familiarizing is of an advantage |
| Comments | A certificate of participation will be handed out Film and sound recordings during the course are strictly forbidden (recorders may be confiscated) |
| Weblink | Department of Pharmaceutical Sciences |
| Admission requirements | Pre-registration by writing an email to studienkoordination-pharma@unibas.ch is mandatory. Enrolled student at the Department of Pharmaceutical Sciences. |
| Course application | Due to a limited number of seats and the Swissethics certification of the course a pre-registration by writing an email to studienkoordination-pharma@unibas.ch is mandatory. |
| Language of instruction | English |
| Use of digital media | No specific media used |
| Interval | Weekday | Time | Room |
|---|---|---|---|
| täglich | See individual dates | ||
| Comments | Findet am SwissTPH in Allschwil statt |
Dates
| Date | Time | Room |
|---|---|---|
| Tuesday 19.01.2027 | 08.45-17.00 | Swiss TPH Neubau, Seminarraum 4 |
| Tuesday 19.01.2027 | 08.45-17.00 | Swiss TPH Neubau, Seminarraum 5 |
| Wednesday 20.01.2027 | 08.45-17.00 | Swiss TPH Neubau, Seminarraum 4 |
| Wednesday 20.01.2027 | 08.45-17.00 | Swiss TPH Neubau, Seminarraum 5 |
| Modules |
Module: Clinical Drug Development: the Basis for Market Approval (Master's Studies: Drug Sciences) |
| Assessment format | continuous assessment |
| Assessment details | Complete participation and 70% correct answers in the multiple choice test (self-checking of acquired knowledge) at the end of the seminar |
| Assessment registration/deregistration | Reg.: course registration, dereg: cancel course registration |
| Repeat examination | no repeat examination |
| Scale | Pass / Fail |
| Repeated registration | as often as necessary |
| Responsible faculty | Faculty of Science, studiendekanat-philnat@unibas.ch |
| Offered by | Departement Pharmazeutische Wissenschaften |