Literature DB >> 24452627

Presumed safe no more: lessons from the Wingspan saga on regulation of devices.

Ari J Gartenberg1, Ariel Peleg, Sanket S Dhruva, Rita F Redberg.   

Abstract

Mesh：

Year:  2014        PMID： 24452627     DOI： 10.1136/bmj.g93

Source DB:  PubMed          Journal:  BMJ        ISSN： 0959-8138


× No keyword cloud information.
  4 in total

1.  Medical device postapproval safety monitoring: where does the United States stand?

Authors:  Prashant V Rajan; Daniel B Kramer; Aaron S Kesselheim
Journal:  Circ Cardiovasc Qual Outcomes       Date:  2015-01-06

2.  Post-market clinical research conducted by medical device manufacturers: a cross-sectional survey.

Authors:  Joseph S Ross; Katrina L Blount; Jessica D Ritchie; Beth Hodshon; Harlan M Krumholz
Journal:  Med Devices (Auckl)       Date:  2015-05-27

3.  Comparison of rates of safety issues and reporting of trial outcomes for medical devices approved in the European Union and United States: cohort study.

Authors:  Thomas J Hwang; Elisaveta Sokolov; Jessica M Franklin; Aaron S Kesselheim
Journal:  BMJ       Date:  2016-06-28

4.  An in Vitro Twist Fatigue Test of Fabric Stent-Grafts Supported by Z-Stents vs. Ringed Stents.

Authors:  Jing Lin; Robert Guidoin; Jia Du; Lu Wang; Graeham Douglas; Danjie Zhu; Mark Nutley; Lygia Perron; Ze Zhang; Yvan Douville
Journal:  Materials (Basel)       Date:  2016-02-16       Impact factor: 3.623
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.