Product description
This course provides a comprehensive overview of Ethics in Clinical Research, covering the ethical foundations, regulatory frameworks, and practical applications essential for conducting responsible clinical studies. It explores core ethical principles, historical milestones, and international guidelines governing human subject research.
Learners will gain in-depth understanding of informed consent, participant protection, and ethical decision-making across different trial phases.
The course also addresses global and national regulations, including harmonization guidelines and country-specific requirements.
International students: Click here to Pay the Fee for this course in US dollars.
Product content
- Welcome to the Course 'Ethics in Clinical Research'
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Announcements
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Course Discussion Forum
- Chapter 1 - Ethics in Clinical Research
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Assessment (C1-ECR)
- Chapter 2 - Informed Consent Process
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Assessment (C2-ICP)
- Chapter 3 - International Conference for Harmonization
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Assessment (C3-ICH)
- Chapter 4 - Schedule-Y
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Assessment (C4-SY)
- Chapter 5 - ICMR Guidelines
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Assessment (C5-ICMR)
- Course Completion
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Final Assessment
