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<http://schema.org/description>
"The topics of this course are divided into 2 parts: The online part will cover the theoretical background and requirements for a clinical study protocol. In the classroom part, the practical aspects and cases will be discussed, including existing regulatory requirements and support. Here you will learn how important it is to have a decent study design, based on sound feasibility.  You will also learn all stakeholders involved in protocol development, yes also patients! Using practical examples and workshops you will learn best practices to match theory with practice. This course focuses on interventional clinical studies."
<https://eccrt.com/courses/designing-clinical-research-protocols-for-a-better-outcome/>