
This course has been accredited by tropEd Network for Higher Education Institutions in International Health.
Next Dates: February 13 - 17, 2023
Course Language: English
Registration: Please register here.
Registration Deadline: January 29, 2023
Course credits: 3 ECTS
Costs: EUR 600
Location: Tuerkenstrasse 89, 80799 Munich, Germany (hybrid considered eventually)
CME points will be applied for.
Content:
- Clinical studies designs and fundamentals of data analysis
- Protocol development
- Case report form (CRF) development
- Study management
- Study outcomes and impact
Learning Objectives:
At the end of the module, the participants will be able to:
- develop a clinical trial protocol (incl. formulation of research question and its primary study objectives; identification of a suitable study design; statistical considerations, etc.),
- design a Case Report Form (CRF) to demonstrate understanding of Clinical Data Management,
- discuss the elements of the clinical trial life cycle and its management (e.g. regulatory and ethical frameworks, timelines and milestones, project execution, quality management tracking and controlling),
- distinguish between different study designs in clinical research (observational studies, e.g. descriptive or cross-sectional studies versus experimental studies, e.g. trial), and
- infer ways to utilize clinical trial findings (e.g. for policy development).
Registration:
If you would like to participate, please register here.
Cancellation policy: For cancellations made before the registration deadline, a non-refundable fee of 100 EUR will be charged. For cancellations made after the registration deadline until the course start, a non-refundable fee of 300 EUR will be charged. In case of no-shows or cancellations from the start of the course, the full course fee will be charged.