The presentations listed below may be reviewed to help you get started in understanding clinical research requirements and responsibilities.
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Introduction to Clinical Research
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Clinical Trial Phases - Design of Clinical Trials
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Protocol Development
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Informed Consent
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Regulatory Framework and Guidelines
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Principal Investigator Responsibilities
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Roles and Responsibilities in Clinical Research
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Monitoring and Reporting
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Data Management and Analysis
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Ethics In Clinical Research
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Clinical Research - Working with UTSW Requirements
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Resources