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JAMA|August 16, 2017
Characteristics of Clinical Studies Used for US Food and Drug Administration Approval of High-Risk Medical Device SupplementsSarah Y Zheng, Sanket S Dhruva, Rita F RedbergMedicine|October 7, 2018
Evidence supporting FDA approval and CMS national coverage determinations for novel medical products, 2005 through 2016: A cross-sectional studyAliya C Roginiel, Sanket S Dhruva, Joseph S RossJAMA|December 31, 2009
Strength of study evidence examined by the FDA in premarket approval of cardiovascular devicesSanket S Dhruva, Lisa A Bero, Rita F RedbergCirculation. Cardiovascular Quality and Outcomes|March 3, 2011
Gender bias in studies for Food and Drug Administration premarket approval of cardiovascular devicesSanket S Dhruva, Lisa A Bero, Rita F RedbergThe American Journal of Managed Care|April 11, 2024
Prices and complications in hospital-based and freestanding surgery centersJames C Robinson, Christopher M Whaley, Sanket S DhruvaNPJ Digital Medicine|December 23, 2022
Characterization of multi-domain postoperative recovery trajectories after cardiac surgery using a digital platformMakoto Mori, Sanket S Dhruva, Arnar Geirsson, et al.JAMA Internal Medicine|September 23, 2016
2016 Update on Medical Overuse: A Systematic ReviewDaniel J Morgan, Sanket S Dhruva, Scott M Wright, et al.JAMA Internal Medicine|November 10, 2015
Update on Medical Practices That Should Be Questioned in 2015Daniel J Morgan, Sanket S Dhruva, Scott M Wright, et al.Journal of the American Heart Association|February 23, 2024
Monitoring of Remotely Reprogrammable Implantable Loop Recorders With Algorithms to Reduce False-Positive AlertsZachary M Neiman, Merritt H Raitt, Gregory Rohrbach, et al.Medical Devices (Auckland, N.Z.)|May 25, 2023
Characterization of US Food and Drug Administration Class I Recalls from 2018 to 2022 for Moderate- and High-Risk Medical Devices: A Cross-Sectional StudyMaryam Mooghali, Joseph S Ross, Kushal T Kadakia, et al.Pageof 20