Clinical Research Ethics: Protecting Patient Rights and Privacy

Rimmalapudi  Kiranmai; Kakada Smruthi

Rimmalapudi Kiranmai Asst.Professor, Vishwanada Insititute of Pharmaceutical Sciences, Vishakhapatnam.
Kakada Smruthi Asst.Professor , VishwanadaInsititute of Pharmaceutical Sciences,Vishakhapatnam

Abstract

Ethical considerations are paramount to ensure the protection of patient rights and privacy throughout the research process. This abstract provides a concise overview of the key principles and practices in clinical research ethics aimed at preserving the well-being of research participants. IRB plays a pivotal role in overseeing the ethical conduct of clinical research. These independent bodies evaluate research proposals, scrutinizing them for adherence to ethical standards and the protection of participant rights. This highlights the interplay of principles, guidelines, and ethical consedirations in clinical research ethics.

Keywords: clinical research, HEC, FDA, HIPPA

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References

1. Principles of Clinical Ethics and Their Application to Practice,
https://doi.org/10.1159/000509119
2. Privacy and Confidentiality, CIRE Current Issues in Research Ethics
https://ccnmtl.columbia.edu/projects/cire/pac/foundation/#3

3. Current Ethical Issues in Healthcare
https://www.floridatechonline.com/blog/healthcare-management/current-ethical-issues-in-healthcare/
4. Protecting Privacy and Confidentiality in Environmental Health Research
Doi: 10.1615/EthicsBiologyEngMed.v1.i4
5. Beauchamp, T. L., & Childress, J. F. (2019). Principles of Biomedical Ethics (8th ed.). Oxford University Press.
6. Emanuel, E. J., Wendler, D., & Grady, C. (2008). What makes clinical research ethical? JAMA, 283(20), 2701-2711.
7. Miller, F. G., & Brody, H. (2013). What makes placebo-controlled trials unethical? American Journal of Bioethics, 3(3), 3-8.