Description
Study Startup is an online eLearning course that provides a practical, end-to-end overview of the clinical study startup process.
It covers study feasibility and site selection, pre-study site visits, site initiation, informed consent, and subject recruitment and retention. Learners will gain hands-on understanding of essential documents, Trial Master File (TMF), and site readiness activities. The course also explains regulatory, ethical, and operational requirements that govern study activation.
By the end, participants will be equipped to efficiently initiate, document, and operationalize clinical trials in compliance with global regulations.
The program is made up of 1 module, 6 topics and 7 Quizzes.
On completing your enrolment for the Study Startup 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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