Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Marie Rape"'
Autor:
Kimberly A. Brownley, Marie Rape, Amanda Wood, Gaurav Dave, Chad Henderson, Diana Severynse-Stevens, Mike Zmuda, Diane Earp, Carmella Moody, Issis Kelly-Pumarol, Joseph Andrews, Kristen M. Foss, Stephanie Fraser, Erika Segear, Amanda B. Parrish
Publikováno v:
Journal of Clinical and Translational Science, Vol 5 (2021)
Availability of trained professionals to assist researchers navigating regulatory pathways for new drug and device development is limited within academic institutions. We created ReGARDD (Regulatory Guidance for Academic Research of Drugs and Devices
Externí odkaz:
https://doaj.org/article/6c525cc4c2a047cfb4a5a506258415f6
Autor:
Jihad S. Obeid, Laura M. Beskow, Marie Rape, Ramkiran Gouripeddi, R. Anthony Black, James J. Cimino, Peter J. Embi, Chunhua Weng, Rebecca Marnocha, John B. Buse, for the Methods and Process and Informatics Domain Task Force Workgroup
Publikováno v:
Journal of Clinical and Translational Science, Vol 1, Pp 246-252 (2017)
Electronic health records (EHRs) provide great promise for identifying cohorts and enhancing research recruitment. Such approaches are sorely needed, but there are few descriptions in the literature of prevailing practices to guide their use. A multi
Externí odkaz:
https://doaj.org/article/cd480d1a998c4b50be750a102d650844
Autor:
Kellie M Walters, Anna Jojic, Emily R Pfaff, Marie Rape, Donald C Spencer, Nicholas J Shaheen, Brent Lamm, Timothy S Carey
Publikováno v:
Journal of the American Medical Informatics Association : JAMIA. 29(4)
Institutions must decide how to manage the use of clinical data to support research while ensuring appropriate protections are in place. Questions about data use and sharing often go beyond what the Health Insurance Portability and Accountability Act
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::62286739fd708bfc968fdeeffc81d25d
https://pubmed.ncbi.nlm.nih.gov/34871428
https://pubmed.ncbi.nlm.nih.gov/34871428
Publikováno v:
J Investig Med
Data and Safety Monitoring Boards (DSMBs) derived from the need to monitor large federally funded multi-center clinical trials and evolved to include commercial and other large and complex trials. Eventually, academic health centers also created inst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b14a8d2bd21730f36abe15377aecf0d
https://pubmed.ncbi.nlm.nih.gov/34074706
https://pubmed.ncbi.nlm.nih.gov/34074706
Autor:
Diana Severynse-Stevens, Kristen M. Foss, Gaurav Dave, Diane Earp, Issis Kelly-Pumarol, Amanda Wood, Erika Segear, Stephanie Fraser, Mike Zmuda, Joseph E. Andrews, Kimberly A Brownley, Amanda B. Parrish, Chad Henderson, Carmella Moody, Marie Rape
Publikováno v:
Journal of Clinical and Translational Science
Availability of trained professionals to assist researchers navigating regulatory pathways for new drug and device development is limited within academic institutions. We created ReGARDD (Regulatory Guidance for Academic Research of Drugs and Devices
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3f1d6c0b7b1c83e5edb5b4e4ca6a0eb4
https://doi.org/10.1017/cts.2021.3
https://doi.org/10.1017/cts.2021.3
Autor:
Marie Rape, Chunhua Weng, Informatics Domain Task Force Workgroup, Laura M. Beskow, R. Anthony Black, Jihad S. Obeid, Ramkiran Gouripeddi, Peter J. Embi, John B. Buse, James J. Cimino, Rebecca Marnocha
Publikováno v:
Journal of Clinical and Translational Science
Electronic health records (EHRs) provide great promise for identifying cohorts and enhancing research recruitment. Such approaches are sorely needed, but there are few descriptions in the literature of prevailing practices to guide their use. A multi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7d1d30bf7c4f43e2bfcd24339a192da1
https://doi.org/10.1017/cts.2017.301
https://doi.org/10.1017/cts.2017.301
Autor:
Mark Stacy, Andreas K. Klein, Aaron Kirby, Marie Rape, Dan M. Cooper, Svetlana Rojevsky, Amy Shepherd, Daniel E. Ford, Robert M. Califf, Joel N. Kline, Norma Terrin, Douglas J. Reichgott, Harry P. Selker, Jonathan M. Davis, Gary E. Rosenthal, Mark S. Wallace, Eric P. Rubinstein, Robert H. Carter, Robert T. O’ Neill, Lisa Guay-Woodford, John B. Buse, Gordon S. Huggins, Amanda Kasper, Pietro Galassetti, Lisa C. Welch, Karl Kieburtz
Publikováno v:
Selker, HP; Buse, JB; Califf, RM; Carter, R; Cooper, DM; Davis, J; et al.(2015). CTSA Consortium Consensus Scientific Review Committee (SRC) Working Group Report on the SRC Processes. Clinical and Translational Science, 8(6), 623-631. doi: 10.1111/cts.12306. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/6pz86134
Clinical and Translational Science
Selker, HP; Buse, JB; Califf, RM; Carter, R; Cooper, DM; Davis, J; et al.(2015). CTSA Consortium Consensus Scientific Review Committee (SRC) Working Group Report on the SRC Processes. Clinical and Translational Science. doi: 10.1111/cts.12306. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/7vt4486v
Clinical and Translational Science, vol 8, iss 6
Clinical and translational science, vol 8, iss 6
Clinical and Translational Science
Selker, HP; Buse, JB; Califf, RM; Carter, R; Cooper, DM; Davis, J; et al.(2015). CTSA Consortium Consensus Scientific Review Committee (SRC) Working Group Report on the SRC Processes. Clinical and Translational Science. doi: 10.1111/cts.12306. UC Irvine: Retrieved from: http://www.escholarship.org/uc/item/7vt4486v
Clinical and Translational Science, vol 8, iss 6
Clinical and translational science, vol 8, iss 6
© 2015 The Authors. Clinical and Translational Science published by Wiley Periodicals, Inc. Human research projects must have a scientifically valid study design, analytic plan, and be operationally feasible in order to be successfully completed and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dbc963781bcc39fb2a29e2014f860743
