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Track 46: Bioethics in Medical Research

Track 46: Bioethics in Medical Research

Overview: Bioethics in Medical Research

Bioethics in medical research refers to the ethical principles and moral considerations that guide the design, conduct, and dissemination of scientific studies involving human participants, animals, or sensitive data. It ensures that research practices uphold human dignity, safety, autonomy, and justice, while promoting scientific integrity. Central to bioethics are principles such as informed consent, beneficence, non-maleficence, confidentiality, and respect for persons. Bioethics also addresses complex issues like genetic manipulation, use of placebos, data privacy, equity in research participation, and fair access to outcomes.

Key Sub-Topics in Bioethics in Medical Research: 

Informed Consent · Human Subject Protection · Ethical Review Boards (IRB/IEC) · Risk-Benefit Analysis · Privacy and Data Confidentiality · Vulnerable Populations in Research · Genetic Ethics · Ethical Use of Placebos · Research Misconduct and Fraud · Cultural Sensitivity in Global Trials · Equity and Access to Research Benefits · Dual-Use Research Concerns · Conflict of Interest Disclosure · Ethics in AI and Digital Health · Publication Ethics