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Site Management and Monitoring in Clinical Trials

Categories: Clinical Trials
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About Course

Learn how clinical trial sites are selected, initiated, monitored, and closed. Focus on GCP-compliant site operations, subject recruitment, and monitoring reports.

What Will You Learn?

  • Understand the 4 Phases of Clinical Trials
  • Learn how protocols are developed and approved
  • Explore the role of ethics committees and informed consent
  • Understand monitoring, data handling, and reporting procedures
  • Know the roles of stakeholders like Sponsors, CROs, and Investigators

Course Content

Clinical Trial Foundations

  • What is a Clinical Trial?
  • History and Evolution of Trials

Clinical Trial Phases

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