Product description
This course provides a comprehensive introduction to the pharmaceutical and clinical research industry, its history, and key milestones.
Learners will explore the roles and responsibilities of stakeholders, ethical foundations, and global regulatory frameworks governing clinical trials. Core principles of Good Clinical Practice (GCP) are emphasized, along with essential trial processes and documentation.
The course also covers emerging technologies in trial management and the importance of safety reporting. Designed as a foundation, it prepares learners for deeper study in advanced clinical research concepts and practices.
International students: Click here to Pay the Fee for this course in US dollars.
Product content
- Welcome to the Course 'Introduction to Clinical Research'
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Announcements
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Course Discussion Forum
- Chapter 1 - Pharmaceutical and Clinical Research Industry Overview
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Assessment (C1-PCRIO)
- Chapter 2 - Introduction to Clinical Research
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Assessment (C2-ICR)
- Chapter 3 - Stakeholders and Roles in Clinical Research
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Assessment (C3-SRCL)
- Chapter 4 - History and Milestones in Clinical Research
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Assessment (C4-HMCR)
- Chapter 5 - Principles of Good Clinical Practice
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Assessment (C5-PGCP)
- Chapter 6 - Technologies in Clinical Trial Management
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Assessment (C6-TCTM)
- Chapter 7 - Overview of Clinical Research Regulatory Bodies
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Assessment (C7-OCRRB)
- Course Completion
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Final Assessment
