Objectives
During the course the student is offered an opportunity to learn all the basic skills needed to plan and execute a clinical drug trial. After passing the study module, the student:
- Understands the phases and flow of clinical drug development studies
- Identifies relevant restrictions and error sources in clinical drug studies
- Can evaluate ethical aspects of a clinical drug trial
- Knows the principles of GCP and the central legislation and regulatory guidance for clinical drug research
- Understands the tasks of different professional groups in the efficient and safe implementation of a clinical drug study
- Is able to compile a protocol for a clinical drug trial
- Understands the basics of statistical analysis applicable in clinical trials
- Can critically interpret publications on clinical drug trials.
During the course the student is offered an opportunity to learn all the basic skills needed to plan and execute a clinical drug trial. After passing the study module, the student:
- Understands the phases and flow of clinical drug development studies
- Identifies relevant restrictions and error sources in clinical drug studies
- Can evaluate ethical aspects of a clinical drug trial
- Knows the principles of GCP and the central legislation and regulatory guidance for clinical drug research
- Understands the tasks of different professional groups in the efficient and safe implementation of a clinical drug study
- Is able to compile a protocol for a clinical drug trial
- Understands the basics of statistical analysis applicable in clinical trials
- Can critically interpret publications on clinical drug trials.
- Opettaja
Päivi Hirvensalo