The role of the U.S. Food and Drug Administration in device evaluation and monitoring-Reference-Cited by-同舟云学术

The role of the U.S. Food and Drug Administration in device evaluation and monitoring

Published:2010-07 Issue:1 Volume:72 Page:5-10
ISSN:0016-5107
Container-title:Gastrointestinal Endoscopy
language:en
Short-container-title:Gastrointestinal Endoscopy

Author:

Diehl David L.,Tierney William M.,Adler Douglas G.,Conway Jason D.,Farraye Francis A.,Kantsevoy Sergey V.,Kaul Vivek,Kethu Sripathi R.,Kwon Richard S.,Mamula Petar,Pedrosa Marcos C.,Rodriguez Sarah A.

Publisher

Elsevier BV

Subject

Gastroenterology,Radiology Nuclear Medicine and imaging

Reference6 articles.

1. Primer on medical device regulation;Monsein;Radiology,1997

2. Institute of Medicine,2005

3. Medical Device regulation: an introduction for the practicing physician;Maisel;Ann Intern Med,2004

4. In F.D.A. files, claims of rush to approve devices;Harris,2009

5. Primer on Medical Device Regulation;Monsein;Radiology,1997

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Analysis of the renewed European Medical Device Regulations in the frame of the non – EU regulatory landscape during the COVID facilitated change;Journal of Pharmaceutical Sciences;2022-10

2. When it comes to surgical devices, what is really broken?;The American Journal of Surgery;2021-06

3. Regulação de dispositivos médicos: vigilância pós-mercado como estratégia de gerenciamento de riscos;Vigilância Sanitária em Debate;2019-11-29

4. Other considerations: Perspective and obligations of our societies and governmental organizations;Techniques in Gastrointestinal Endoscopy;2019-10

5. Endoscopes, Guidewires, and Accessories;ERCP;2019