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In this course, you will :
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Understand the process for designing and running clinical trials on medical devices
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Understand the rights of patients and the responsibilities of sponsors and investigators
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Combine this knowledge with personal experience to pass the various clinical research certification exams
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Become familiar with Good Clinical Practices (GCP's)
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Understand and summarize clinical research regulations such as the ICH guidelines and 21 CFR parts 50, 56, and 812
