| Literature DB >> 34192287 |
Laura Gibson1, Nisha Fahey1, Nathaniel Hafer1, Bryan Buchholz2, Denise Dunlap2, Robert Murphy3, Chad Achenbach3, Cheryl Stone4, Rebecca Cleeton4, Jared O'Neal5, Jennifer Frediani6, Miriam Vos5, Oliver Brand7, Risha Nayee5, Leona Wells5, Wilbur Lam5, Greg Martin5, Yukari Manabe8, Matthew Robinson8, John Broach1, Jeffrey Olgin9, Bruce Barton1, Stephenie Lemon1, Allison Blodgett1, David McManus1.
Abstract
The National Institutes of Health (NIH) launched the Rapid Acceleration of Diagnostics (RADxSM) 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. This work is licensed under a Creative Commons Attribution 4.0 License. For more information, see https://creativecommons.org/licenses/by/4.0/.Entities:
Keywords: COVID-19; SARS-CoV-2; [Formula: see text] diagnostics; point-of-care testing; rapid acceleration of diagnostics
Year: 2021 PMID: 34192287 PMCID: PMC8112667 DOI: 10.1109/OJEMB.2021.3070830
Source DB: PubMed Journal: IEEE Open J Eng Med Biol ISSN: 2644-1276