Applied Clinical Research

This course has been accredited by tropEd Network for Higher Education Institutions in International Health.

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.