| 1 |
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Introduction to Clinical Study and Evaluation |
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| 2 |
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Responsibilities for conducting the research |
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| 3 |
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Responsibilities of Research Product |
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| 4 |
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Responsibilities Regarding Data and Records |
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| 5 |
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Responsibilities of Contract Research Organization |
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| 6 |
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Monitoring in Clinical Drug Research |
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| 7 |
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Audience Selection and Characteristics |
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| 8 |
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MID-TERM EXAM |
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| 9 |
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Quality Control and Quality Assurance in Clinical Drug Research |
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| 10 |
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Coverage of Damages Caused by Clinical Drug Research |
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| 11 |
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Overview of the Structure of Bioethics Committees |
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| 12 |
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Council of Europe and Medical Research on People |
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| 13 |
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Duties and Functioning of Clinical Research Ethics Committees |
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| 14 |
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Student Presentations - Question and Answer |
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| 15 |
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An overview |
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| 16 |
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FINAL EXAM |
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| 17 |
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FINAL EXAM |
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