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.
Indian students: Choose the Offline Payment option at Checkout. Once your Order is created you will receive an email with a link to complete your payment of INR 19,999.
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
