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The Informed Consent Resource
Explore the basic elements of informed consent that are required by the Common Rule and that are relevant to genomics.
Policy Issues
El uso de seres humanos en las investigaciones biomédicas, clínicas y socioconductuales puede ofrecer entendimiento y descubrimientos que no pudieran obtenerse de ninguna otra manera.
Policy Issues
Revisions to the Common Rule modernize, simplify, and enhance oversight for human subjects research in the United States.
Policy Issues
Clinical research may yield new health-related information about volunteers who have chosen to participate in the studies.
Policy Issues
Federally-funded research with human participants must comply with regulations that protect the rights and welfare of the participants.
Policy Issues
NHGRI wants to ensure that all populations benefit from the advances of genomics research.
Policy Issues
Scientific institutions are developing recommendations to support the responsible use of human gene-editing research.
Policy Issues
Patients with genetic disorders and members of the public have diverse about germline genome editing.
Policy Issues
Most ethical discussions about genome editing center on human germline editing because changes are passed down to future generations.
Policy Issues
Genome editing is currently being applied to research on cancer, mental health, rare diseases, and many other disease areas.