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Clinical Trials (London, England)|April 17, 2021
US Food and Drug Administration utilization of postmarketing requirements and postmarketing commitments, 2009-2018Joshua J Skydel, Audrey D Zhang, Sanket S Dhruva, et al.
Ophthalmology|May 15, 2017
Incremental Revisions across the Life Span of Ophthalmic Devices after Initial Food and Drug Administration Premarket Approval, 1979-2015Anand D Gopal, Vinay K Rathi, Christopher C Teng, et al.
BMJ Surgery, Interventions, & Health Technologies|January 27, 2023
Exploring unique device identifier implementation and use for real-world evidence: a mixed-methods study with NESTcc health system network collaboratorsSanket S Dhruva, Jennifer L Ridgeway, Joseph S Ross, et al.
JAMA Internal Medicine|December 8, 2025
Postmarket Drug Safety-Related Actions Before and After the US Food and Drug Administration Amendments ActHarry Doernberg, Joshua D Wallach, Molly M Jeffery, et al.
BMJ (Clinical Research Ed.)|March 13, 2025
Late adverse event reporting from medical device manufacturers to the US Food and Drug Administration: cross sectional studyAlexander O Everhart, Pinar Karaca-Mandic, Rita F Redberg, et al.
Health Affairs (Project Hope)|August 10, 2016
Racial Disparities In Geographic Access To Primary Care In PhiladelphiaElizabeth J Brown, Daniel Polsky, Corentin M Barbu, et al.
American Journal of Public Health|June 30, 2017
Effect of Outreach Messages on Medicaid EnrollmentJeffrey K Hom, Christian Stillson, Roy Rosin, et al.
The American Journal of Managed Care|August 30, 2017
Twitter accounts followed by Congressional health staffDavid Grande, Zachary F Meisel, Raina M Merchant, et al.
Journal of Hospital Medicine|December 6, 2012
Perceptions of readmitted patients on the transition from hospital to homeShreya Kangovi, David Grande, Patricia Meehan, et al.
Health Affairs (Project Hope)|December 10, 2014
Lessons for providers and hospitals from Philadelphia's obstetric services closures and consolidations, 1997-2012Scott A Lorch, Ashley E Martin, Richa Ranade, et al.
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