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Certificate Course in Medico-Legal Aspects of Clinical Studies

Categories: Medico-Legal
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What Will You Learn?

  • Understanding Regulatory Frameworks: Gain comprehensive knowledge of the legal and ethical guidelines governing clinical studies, ensuring compliance with national standards.
  • Informed Consent and Patient Rights: Learn the intricacies of obtaining valid informed consent and safeguarding patient rights.
  • Risk Management and Liability: Explore strategies to identify, assess, and mitigate legal risks in clinical studies, including handling potential liabilities.
  • Case Studies and Legal Precedents: Analyze real-world cases and legal precedents to understand the implications of medico-legal issues in clinical research.

Course Content

Module 1: Medicolegal Primer

  • Lesson
    35:09

Module 2: Consumer Protection Act 2019

Module 3: When you get a legal notice

Module 4: Deficiencies in Consent in Gastroenterology

Module 5: Communication

Module 6: Communication after a Complicated Endoscopy

Module 7: Documentation

Module 8: Death on Table

Module 9: Medicolegal workshop in Gastroenterology and GI emergencies (Case Scenarios)

Module 10: Telemedicine

Module 11: Residents’ Liability