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Health Affairs Scholar|July 13, 2026
Reforming Medicare payment for skin substitutes-ripping off the bandageJad F Zeitouni, Xiaodan Hu, Sanket S Dhruva, et al.
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.
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.
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.
Journal of Managed Care & Specialty Pharmacy|October 31, 2019
Medicare Prescription Drug Plan Formulary Restrictions After Postmarket FDA Black Box WarningsMichael T Solotke, Joseph S Ross, Nilay D Shah, et al.
The Milbank Quarterly|December 27, 2022
A Policy Approach to Reducing Low-Value Device-Based Procedure UseSanket S Dhruva, Marcus A Bachhuber, Ashwin Shetty, et al.
Annals of Internal Medicine|October 7, 2024
Modernizing Medical Device Regulation: Challenges and Opportunities for the 510(k) Clearance ProcessKushal T Kadakia, Vinay K Rathi, Sanket S Dhruva, et al.
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