Clinical Trials Committees: How Long Is the Protocol Review and Approval Process in Spain? A Prospective Study

&
IRB: Ethics & Human Research 17 (4):6 (1995)
  Copy   BIBTEX

Abstract

This article has no associated abstract. (fix it)

Categories

Keywords

Reprint years

DOI

10.2307/3564154

Other Versions

No versions found

Links

PhilArchive



    Upload a copy of this work     Papers currently archived: 103,449

External links

Setup an account with your affiliations in order to access resources via your University's proxy server

Through your library

My notes

Similar books and articles

Performance of research ethics committees in Spain. A prospective study of 100 applications for clinical trial protocols on medicines.R. Dal-Re, J. Espada & R. Ortega - 1999 - Journal of Medical Ethics 25 (3):268-273.
Toward Prospective Registration of Clinical Trials.Curtis L. Meinert - 1988 - IRB: Ethics & Human Research 10 (2):6.
No, Not Another IRBData Monitoring Committees in Clinical Trials: A Practical Perspective.Bruce Levin, Susan S. Ellenberg, Thomas R. Fleming & David L. DeMets - 2003 - IRB: Ethics & Human Research 25 (1):17.
The Role of Community Advisory Committees in Clinical Trials of Anti-HIV Agents.Ronald O. Valdiserri, Geraldine Maiatico Tama & Monto Ho - 1988 - IRB: Ethics & Human Research 10 (4):5.
Ethical Issues Arising When Interim Data in Clinical Trials Is Restricted to Independent Data Monitoring Committees.Robert J. Wells, Peter S. Gartside & Christine L. McHenry - 2000 - IRB: Ethics & Human Research 22 (1):7.
Scientific Design, Ethics, and Monitoring: IRB Review of Randomized Clinical Trials. [REVIEW]Dale H. Cowan - 1980 - IRB: Ethics & Human Research 2 (9):1.
Improving the Ethics of Clinical Trials: The Case of an 'Add-on' Study.Michael Weintraub - 1983 - IRB: Ethics & Human Research 5 (3):7.
A case study in adolescent participation in clinical research: eleven clinical sites, one common protocol, and eleven IRBs.Audrey Smith Rogers, Donald F. Schwartz, Gloria Weissman & A. English - 1998 - IRB: Ethics & Human Research 21 (1):6-10.
Incorporating ethical principles into clinical research protocols: a tool for protocol writers and ethics committees.Rebecca H. Li, Mary C. Wacholtz, Mark Barnes, Liam Boggs, Susan Callery-D'Amico, Amy Davis, Alla Digilova, David Forster, Kate Heffernan, Maeve Luthin, Holly Fernandez Lynch, Lindsay McNair, Jennifer E. Miller, Jacquelyn Murphy, Luann Van Campen, Mark Wilenzick, Delia Wolf, Cris Woolston, Carmen Aldinger & Barbara E. Bierer - 2016 - Journal of Medical Ethics 42 (4):229-234.

Analytics

Added to PP
2014-03-27

Downloads
17 (#1,196,561)

6 months
3 (#1,061,821)

Historical graph of downloads
How can I increase my downloads?

Author's Profile

Citations of this work

Add more citations

References found in this work

No references found.

Add more references