FRM5730 – Clinical Drug Trials
Course description
Course content
Learning outcome
The course is intended to provide the relevant and fundamental information to those who, in one way or another, plan to be involved with clinical trials. During the course, the students are to acquire the necessary information in the following areas:
- Fundamental theory concerning clinical drug trials
- Ethical issues
- Safety reporting
- Research methodology
- GCP (Good Clinical Practice)
- The handling of medicine
- Evaluating the results
- Evaluating the statistics
- Quality assurance
Admission to the course
Formal prerequisite knowledge
Overlapping courses
- 10 credits overlap with FRM9730 – Clinical Drug Trials (discontinued).
- 5 credits overlap with FARM4120 – Drug Development.
Teaching
Lectures, seminars, and compulsory group assignments.
The majority of the course will be taught through lectures and seminars, and will cover the design and planning of clinical testing of medicine. The students are expected to work in groups of 3-4 and write a clinical trial protocol, as well as determine which officials or institutions one needs to apply to in order to start a clinical trial.
Inactivity and / or excessive absences in compulsory education means that the student does not receive final assessment / examination
Examination
Examination support material
Grading scale
Resit an examination
This course offers both postponed and resit of examination. Read more:
More about examinations at UiO
- Use of sources and citations
- How to use AI as a student
- Special exam arrangements due to individual needs
- Withdrawal from an exam
- Illness at exams / postponed exams
- Explanation of grades and appeals
- Resitting an exam
- Cheating/attempted cheating
You will find further guides and resources at the web page on examinations at UiO.