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dc.contributor.authorGibson, Laura L.
dc.contributor.authorFahey, Nisha M.
dc.contributor.authorHafer, Nathaniel
dc.contributor.authorBroach, John P.
dc.contributor.authorBarton, Bruce A.
dc.contributor.authorLemon, Stephenie C.
dc.contributor.authorBlodgett, Allison
dc.contributor.authorMcManus, David D.
dc.date2022-08-11T08:09:59.000
dc.date.accessioned2022-08-23T16:51:06Z
dc.date.available2022-08-23T16:51:06Z
dc.date.issued2021-04-28
dc.date.submitted2021-05-05
dc.identifier.citation<p>L. L. Gibson et al., "The RADx Tech Clinical Studies Core: A Model for Academic Based Clinical Studies," in IEEE Open Journal of Engineering in Medicine and Biology, vol. 2, pp. 152-157, 2021, doi: 10.1109/OJEMB.2021.3070830. <a href="https://doi.org/10.1109/OJEMB.2021.3070830" target="_blank" title="view article on publisher's site">View article on publisher's site</a></p>
dc.identifier.doi10.1109/OJEMB.2021.3070830
dc.identifier.pmid34192287
dc.identifier.urihttp://hdl.handle.net/20.500.14038/41794
dc.description<p>Full author list omitted for brevity. For the full list of authors, see article.</p>
dc.description.abstractThe National Institutes of Health (NIH) launched the Rapid Acceleration of Diagnostics (RADx SM ) Tech initiative to support the development and commercialization of novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) point-of-care test devices. The primary objective of the Clinical Studies Core (CSC) was to perform SARS-CoV-2 device studies involving diverse populations and settings. Within a few months, the infrastructure for clinical studies was developed, including a master protocol, digital study platform, data management system, single IRB, and multi-site partnerships. Data from some studies are being used to support Emergency Use Authorization of novel SARS-CoV-2 test devices. The CSC reduced the typical time and cost of developing medical devices and highlighted the impactful role of academic and NIH partnership in addressing public health needs at a rapid pace during a global pandemic. The structure, deployment, and lessons learned from this experience are widely applicable to future in vitro diagnostic device clinical studies.
dc.language.isoen_US
dc.rightsThis work is licensed under a Creative Commons Attribution 4.0 License. For more information, see https://creativecommons.org/licenses/by/4.0/
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectSARS-CoV-2
dc.subjectCOVID-19
dc.subjectin vitro diagnostics
dc.subjectpoint-of-care testing
dc.subjectrapid acceleration of diagnostics
dc.subjectUMCCTS funding
dc.subjectBiomedical Engineering and Bioengineering
dc.subjectDiagnosis
dc.subjectHealth and Medical Administration
dc.subjectInfectious Disease
dc.subjectTranslational Medical Research
dc.subjectVirus Diseases
dc.titleThe RADx Tech Clinical Studies Core: A Model for Academic Based Clinical Studies
dc.typeJournal Article
dc.source.journaltitleIEEE Open Journal of Engineering in Medicine and Biology
dc.source.volume2
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=5624&amp;context=oapubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/oapubs/4594
dc.identifier.contextkey22798775
refterms.dateFOA2022-08-23T16:51:06Z
html.description.abstract<p>The National Institutes of Health (NIH) launched the Rapid Acceleration of Diagnostics (RADx <sup>SM</sup> ) Tech initiative to support the development and commercialization of novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) point-of-care test devices. The primary objective of the Clinical Studies Core (CSC) was to perform SARS-CoV-2 device studies involving diverse populations and settings. Within a few months, the infrastructure for clinical studies was developed, including a master protocol, digital study platform, data management system, single IRB, and multi-site partnerships. Data from some studies are being used to support Emergency Use Authorization of novel SARS-CoV-2 test devices. The CSC reduced the typical time and cost of developing medical devices and highlighted the impactful role of academic and NIH partnership in addressing public health needs at a rapid pace during a global pandemic. The structure, deployment, and lessons learned from this experience are widely applicable to future in vitro diagnostic device clinical studies.</p>
dc.identifier.submissionpathoapubs/4594
dc.contributor.departmentUMass Worcester Prevention Research Center
dc.contributor.departmentDepartment of Medicine, Division of Cardiovascular Medicine
dc.contributor.departmentGraduate School of Nursing
dc.contributor.departmentDepartment of Population and Quantitative Health Sciences
dc.contributor.departmentDepartment of Emergency Medicine
dc.contributor.departmentUMass Center for Clinical and Translational Science
dc.contributor.departmentDepartment of Pediatrics
dc.contributor.departmentDepartment of Medicine, Division of Infectious Diseases and Immunology
dc.source.pages152-157


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This work is licensed under a Creative Commons Attribution 4.0 License. For more information, see https://creativecommons.org/licenses/by/4.0/
Except where otherwise noted, this item's license is described as This work is licensed under a Creative Commons Attribution 4.0 License. For more information, see https://creativecommons.org/licenses/by/4.0/