Pinar Karaca-Mandic

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Late adverse event reporting from medical device manufacturers to the US Food and Drug Administration: cross sectional study

1 month ago | bmj.com | Alexander O. Everhart |Pinar Karaca-Mandic |Rita F. Redberg |Joseph Ross

Research BMJ 2025; 388 doi: https://doi.org/10.1136/bmj-2024-081518 Cite this as: BMJ 2025;388:e081518 Alexander O Everhart, instructor1 2, Pinar Karaca-Mandic, professor3, Rita F Redberg, professor4 5, Joseph S Ross, professor6 7 8, Sanket S Dhruva, associate professor9 10 11 1Division of General Medical Sciences, John T Milliken Department of Medicine, Washington University School of Medicine in St Louis, St Louis, MO, USA 2Center for Advancing Health Services, Policy and Economics...

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