Description
Clinical Trial Preparation is an online eLearning course that covers the core areas of Protocol Development and CRF Design as part of preparation to commence a clinical trial.
This course is designed to help learners clearly understand how clinical trials are prepared before they begin. The course explains key activities such as writing clinical study protocols, designing Case Report Forms (CRFs), and meeting ethical and regulatory requirements. It also outlines the roles and responsibilities of different stakeholders involved in trial preparation. Strong focus is placed on documentation, data quality, and regulatory compliance. By the end of the module, learners will be well prepared to move confidently from trial planning to actual study execution.
The program is made up of 1 module, 2 topics and 3 Quizzes.
On completing your enrolment for the Clinical Trial Preparation program you will instantly get access to our online learning portal.
Find more information about the field of Clinical Research –Â What is Clinical Research
Looking for a comprehensive program in Clinical Research? Explore our Diploma in Clinical Research program.
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