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Publication
Race & research: Perspectives on minority participation in health studies
American Public Health Association PressDigital citation created by the Bioethics Research Library, Georgetown University, for the National Information Resource on Ethics and Human Genetics, a project funded by the United States National… -
Publication
Pharmaceuticals, biotechnology & the law
MacmillanDigital citation created by the Bioethics Research Library, Georgetown University, for the National Information Resource on Ethics and Human Genetics, a project funded by the United States National… -
Publication
Biological anthropology and ethics: From repatriation to genetic identity
State University of New York PressDigital citation created by the Bioethics Research Library, Georgetown University, for the National Information Resource on Ethics and Human Genetics, a project funded by the United States National… -
Publication
Legal constraints on the use of race in biomedical research: Toward a social justice framework
Journal of Law, Medicine & EthicsDigital citation created by the Bioethics Research Library, Georgetown University, for the National Information Resource on Ethics and Human Genetics, a project funded by the United States National… -
Publication
The role of patients and patient advocacy groups in educating patients on the importance of legitimate scientific research
American Journal of BioethicsDigital citation created by the Bioethics Research Library, Georgetown University, for the National Information Resource on Ethics and Human Genetics, a project funded by the United States National… -
Additional Resource
Nevada State Statute (Nevada: NRS §629.101 et seq.)
It is unlawful to obtain any genetic information of a person without informed consent with some exceptions, including for use in a study where the identities of the persons from whom the genetic…- state statute
- Nevada
- genetic privacy
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Grant Abstract
Implications of Genome Research: A Model College Course
This project will develop a new multidisciplinary undergraduate course in the ethical, legal, and social implications of the Human Genome Project. The course will offer a case-study oriented approach…- behavioral /social science research tag
- biotechnology
- curriculum
- Education
- education evaluation /planning
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Grant Abstract
Implications of Genome Research: A Summer Institute
During each of the summers of 2000, 2001 and 2002, Dartmouth's Ethics Institute proposes to offer a Faculty Institute to a group of 20 college and university teachers in order to prepare them to…- behavioral /social science research tag
- biotechnology
- curriculum
- Education
- education evaluation /planning
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Additional Resource
Minnesota State Statute (Minnesota: MS §72A.139)
A health plan company in determining eligibility for coverage, establishing premiums, limiting coverage, renewing coverage, or any other underwriting decision may not (1) require or request an…- state statute
- Minnesota
- health insurance nondiscrimination
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Additional Resource
Massachusetts 2011 State Bills (Massachusetts 2011 S 1080)
This bill creates the Genetic Bill of RIghts. Genetic information is declared the exclusive property of the individual from whom the information is obtained. The bill also prohibits disclosure of…- state bill
- bill
- bill status died
- Massachusetts
- health insurance nondiscrimination