Investigator perception of trial presentation to the clinical research ethics committee

2012 ◽  
Vol 19 (2) ◽  
pp. 241.2-241
Author(s):  
N. Vilardell ◽  
S. Redondo ◽  
N. Giménez ◽  
L. Soriano ◽  
R. Pla ◽  
...  
Keyword(s):  
Clinical Research ◽  
Research Ethics ◽  
Ethics Committee ◽  
Research Ethics Committee

scholarly journals A Comparison of Clinical Research Ethics Committee between Japan and Foreign Countries

2018 ◽  
Vol WCP2018 (0) ◽  
pp. PO1-13-5
Author(s):  
Yuka Onaka ◽  
Naoko Kitada ◽  
Hiromi Umezome ◽  
Shoko Tanaka ◽  
Akiko Okumura ◽  
...  
Keyword(s):  
Clinical Research ◽  
Research Ethics ◽  
Ethics Committee ◽  
Research Ethics Committee ◽  
Foreign Countries

scholarly journals The Spectrum of Clinical Research with Medications in A Spanish University Hospital. Review of 1.000 Clinical Trials Evaluated by the Research Ethics Committee

2009 ◽  
Vol 3 (1) ◽  
pp. 20-27
Author(s):  
Emma Fernandez de Uzquiano ◽  
A. Gil Aguado ◽  
P. Lavilla Uriol ◽  
J. Frias Iniesta ◽  
R. Madero Jarabo ◽  
...  
Keyword(s):  
Clinical Trials ◽  
Clinical Research ◽  
Research Ethics ◽  
Ethics Committee ◽  
University Hospital ◽  
Research Ethics Committee

scholarly journals Citizens, Research Ethics Committee Members and Researchers’ Attitude Toward Information and Consent for the Secondary Use of Health Data: Implications for Research Within Learning Health Systems

2021 ◽  
pp. 155626462199221
Author(s):  
Annabelle Cumyn ◽  
Roxanne Dault ◽  
Adrien Barton ◽  
Anne-Marie Cloutier ◽  
Jean-François Ethier
Keyword(s):  
Research Ethics ◽  
Health Systems ◽  
Ethics Committee ◽  
Health Data ◽  
Data Reuse ◽  
Fundamental Importance ◽  
Research Ethics Committee ◽  
Secondary Use ◽  
Public Perspectives ◽  
Advance Knowledge

A survey was conducted to assess citizens, research ethics committee members, and researchers’ attitude toward information and consent for the secondary use of health data for research within learning health systems (LHSs). Results show that the reuse of health data for research to advance knowledge and improve care is valued by all parties; consent regarding health data reuse for research has fundamental importance particularly to citizens; and all respondents deemed important the existence of a secure website to support the information and consent processes. This survey was part of a larger project that aims at exploring public perspectives on alternate approaches to the current consent models for health data reuse to take into consideration the unique features of LHSs. The revised model will need to ensure that citizens are given the opportunity to be better informed about upcoming research and have their say, when possible, in the use of their data.

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