Registry and results database of publicly and privately supported clinical studies of human participants conducted around the world. A service of the U.S. National Institutes of Health
A body of 36 independent experts that follows progress in the life sciences and its applications in order to ensure respect for human dignity and freedom. It was created in 1993.
Provides leadership in the protection of the rights, welfare, and wellbeing of subjects involved in research conducted or supported by the U.S. Department of Health and Human Services.
Bioethicists, biomedical policy experts and lawyers, physicians, nursing and allied health students as well as science educators will find this book helpful and engaging in exploring the complexities of modern evolutionary, genetic and biomedical data.
a case-based introduction to ethical issues in health care. Through seventy-eight compelling scenarios, the authors demonstrate the practical importance of ethics, showing how the concerns at issue bear on the lives of patients, health care providers, and others.
This collection represents the contributions of the IBC to global bioethics. The IBC is a body of 36 independent experts that follows progress in the life sciences and its applications in order to ensure respect for human dignity and freedom.
A collection of resources for scientific investigators conducting research in the developing world, and ethics committees reviewing it. From NIH Fogarty International Center
The HIPAA Privacy Rule establishes the conditions under which protected health information may be used or disclosed by covered entities for research purposes. Research is defined in the Privacy Rule as, “a systematic investigation, including research development, testing, and evaluation, designed to develop or contribute to generalizable knowledge.”
Bioethics and the Human Goods by 
A Guide to Bioethics by 
Bioethics : Legal and clinical case studies. by 
Specimen Science by 
Global Bioethics: the Impact of the UNESCO International Bioethics Committee by 