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Ethical Considerations in Clinical Research: Protecting Human Subjects

“Safeguarding Humanity: Ethical Considerations in Clinical Research”

About Program:

Aim: This program aims to familiarize participants with the ethical principles and considerations involved in conducting clinical research. Participants will learn about the ethical framework, guidelines, and regulations governing human subjects’ protection, informed consent, and research integrity.

Program Objectives:

What you will learn?

Week 1: Introduction to Medical Ethics in Clinical Research

  • Overview of medical ethics and its relevance to clinical research
  • Ethical principles and frameworks for research involving human subjects

Week 2: Informed Consent and Participant Autonomy

  • Importance of informed consent and its elements
  • Consent process, capacity assessment, and participant autonomy

Week 3: Ethical Considerations in Study Design

  • Ethical challenges in study design and participant selection
  • Balancing scientific rigor and ethical requirements

Week 4: Privacy, Confidentiality, and Data Protection

  • Maintaining privacy and confidentiality of research participants
  • Ethical considerations in data collection, storage, and sharing

Week 5: Vulnerable Populations and Research Ethics

  • Ethical considerations when involving vulnerable populations
  • Special protections for children, pregnant women, and other vulnerable groups

Week 6: Research Ethics Committees and Institutional Review Boards

  • Role and functions of research ethics committees
  • Ethical review process and criteria for research approval

Week 7: Risk-Benefit Assessment and Minimization

  • Ethical considerations in risk assessment and management
  • Balancing potential benefits and risks for research participants

Week 8: Reporting Adverse Events and Safety Monitoring

  • Ethical responsibilities in adverse event reporting
  • Safety monitoring and pharmacovigilance in clinical research

Week 9: Publication Ethics and Responsible Conduct of Research

  • Ensuring integrity and transparency in research reporting
  • Avoiding plagiarism, data fabrication, and research misconduct

Week 10: International Ethical Guidelines and Cultural Considerations

  • Ethical guidelines and cultural diversity in clinical research
  • Navigating ethical challenges in global research collaborations

Week 11: Ethical Issues in Multi-Center Trials and Data Sharing

  • Ethical considerations in multi-center trials and data sharing
  • Collaboration, authorship, and ownership of research data

Week 12: Ethics in Post-Trial Activities and Dissemination of Results

  • Ethical responsibilities in post-trial activities and long-term follow-up
  • Dissemination of research findings and public engagement

Fee Plan

INR 1999 /- OR USD 50

Get an e-Certificate of Participation!

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Intended For : Graduates, Post Graduates, Research Scholars, Academicians, Industry Professionals of Healthcare and Medical Research Sector

Career Supporting Skills

Clinical Trial Protocol Development Good Clinical Practice (GCP) Guidelines Research Ethics and Regulatory Compliance Policy and Regulatory Compliance Scientific Writing and Communication

Program Outcomes

  • Understanding of ethical principles and guidelines in clinical research.
  • Proficiency in obtaining informed consent and ensuring participant confidentiality.
  • Knowledge of ethical considerations in vulnerable populations.
  • Awareness of research integrity and responsible conduct of research.
  • Competence in ethical decision-making and resolving ethical dilemmas.