Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Leslie E. Wolf"'
Autor:
Justin X. Moore, LaKesha N. Anderson, Cynthia Li, Reginald D. Benson, Alejandra Garcia Rychtarikova, Lillie D. Williamson, Leslie E. Wolf, Ebony B. Whisenant, Erin Roark, Samantha R. Jones, Christy J.W. Ledford
Publikováno v:
Journal of Clinical and Translational Science, Vol 7 (2023)
Externí odkaz:
https://doaj.org/article/dd026de7f87b49098280e85d23b9f881
Publikováno v:
The American Journal of Bioethics. 22:36-38
Autor:
Leslie E Wolf, Erin Fuse Brown, Roxanne Greeson, Catherine Hammack-Aviran, James W Hazel, William Rencher, Laura M Beskow
Publikováno v:
Journal of law and the biosciences. 9(1)
Precision medicine research implicates numerous state laws that may affect participants’ rights and protections and are not preempted by federal law. The choice of which state’s laws apply, and under what circumstances, can have significant impac
Autor:
Laura M. Beskow, Leslie E. Wolf
Publikováno v:
Am J Hum Genet
Large-scale precision medicine research requires massive amounts of data representing people from all walks of life; thus, in the US, it is often multistate research. Significant legal and ethical quandaries arise as a result of the patchwork of laws
Autor:
Leslie E. Wolf, Catherine M. Hammack, Laura M. Beskow, Kathleen M. Brelsford, Erin C. Fuse Brown
Publikováno v:
The Journal of Law, Medicine & Ethics
Researchers now commonly collect biospecimens for genomic analysis together with information from mobile devices and electronic health records. This rich combination of data creates new opportunities for understanding and addressing important health
Publikováno v:
Journal of Law and the Biosciences. 9
Federal law establishes minimum standards for protecting human research participants, but many states have enacted laws that may apply to research. Precision medicine research in particular implicates state laws that govern an array of topics, includ
Publikováno v:
Journal of Law, Medicine & Ethics. 47:213-231
The revised Common Rule includes a new option for the conduct of secondary research with identifiable data and biospecimens: regulatory broad consent. Motivated by concerns regarding autonomy and trust in the research enterprise, regulators had initi
Autor:
Laura M Beskow, Devon K Check, Emily E Namey, Lauren A Dame, Li Lin, Alexandra Cooper, Kevin P Weinfurt, Leslie E Wolf
Publikováno v:
PLoS ONE, Vol 7, Iss 9, p e44050 (2012)
Certificates of Confidentiality, issued by agencies of the U.S. government, are regarded as an important tool for meeting ethical and legal obligations to safeguard research participants' privacy and confidentiality. By shielding against forced discl
Externí odkaz:
https://doaj.org/article/c437b49ac60e48d2923219be4f621c8a
Autor:
Leslie E. Wolf, Laura M. Beskow
Publikováno v:
American Journal of Law & Medicine. 44:343-358
Certificates of Confidentiality (“Certificates”) are a federal legal tool designed to protect sensitive, identifiable research data from compelled disclosure. Congress first authorized their use in 1970 to facilitate research on illegal drug use.
Publikováno v:
PLoS ONE, Vol 2, Iss 10, p e1005 (2007)
In September 2006, the Centers for Disease Control and Prevention (CDC) recommended routine HIV testing for all Americans aged 13-64, which would eliminate requirements for written consent and pretest counseling as previously required. However, this
Externí odkaz:
https://doaj.org/article/29fe523131564ca08cc66df5de124bfb