Paper: Ethical review reporting of Chinese trials records in WHO primary registries

, , , &
Journal of Medical Ethics 37 (3):144-148 (2011)
  Copy   BIBTEX

Abstract

This article has no associated abstract. (fix it)

Categories

Keywords

Reprint years

DOI

10.1136/jme.2010.036558

Links

PhilArchive



    Upload a copy of this work     Papers currently archived: 91,963

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

Reporting of informed consent, standard of care and post‐trial obligations in global randomized intervention trials: A systematic survey of registered trials.Jennifer M. O'neill Emma R. Cohen - 2009 - Developing World Bioethics 9 (2):74-80.
Methodological quality and reporting of ethical requirements in phase III cancer trials.J. J. Tuech - 2005 - Journal of Medical Ethics 31 (5):251-255.
Reporting of informed consent, standard of care and post-trial obligations in global randomized intervention trials: A systematic survey of registered trials.Emma R. M. Cohen, Jennifer M. O'neill, Michel Joffres, Ross E. G. Upshur & Edward Mills - 2008 - Developing World Bioethics 9 (2):74-80.
Selected Issues Related to the Conduct, Reporting, and Analysis of Phase I Trials.Marcelle Denise Winget - 1996 - Dissertation, The Johns Hopkins University
Evaluating solutions to sponsorship bias.M. Doucet & S. Sismondo - 2008 - Journal of Medical Ethics 34 (8):627-630.
Reporting the Study Populations of Clinical Trials. Clear Transmission or Static on the Line?Stanley H. Shapiro, Charles Weijer & Benjamin Freedman - unknown
Reporting of ethical requirements in phase III surgical trials.Valérie Bridoux, Lilian Schwarz, Grégoire Moutel, Francis Michot, Christian Herve & Jean-Jacques Tuech - 2014 - Journal of Medical Ethics 40 (10):687-690.
Medical records: practicalities and principles of patient possession.M. L. Gilhooly & S. M. McGhee - 1991 - Journal of Medical Ethics 17 (3):138-143.
Methodological quality and reporting of ethical requirements in clinical trials.M. Ruiz-Canela - 2001 - Journal of Medical Ethics 27 (3):172-176.
Developing registries of volunteers: key principles to manage issues regarding personal information protection.E. Levesque, D. Leclerc, J. Puymirat & B. M. Knoppers - 2010 - Journal of Medical Ethics 36 (11):712-714.
Can unequal be more fair? A response to Andrew Avins.S. J. L. Edwards - 2000 - Journal of Medical Ethics 26 (3):179-182.
The Role of Consent and Individual Autonomy in the PIP Breast Implant Scandal.B. Schofield - 2013 - Public Health Ethics 6 (2):220-223.
Filling the information void: Using public registries as a tool in nanotechnologies regulation. [REVIEW]Diana M. Bowman & Karinne Ludlow - 2009 - Journal of Bioethical Inquiry 6 (1):25-36.
Poor reporting quality of key Randomization and Allocation Concealment details is still prevalent among published RCTs in 2011: a review.Laura Clark, Ulrike Schmidt, Puvan Tharmanathan, Joy Adamson, Catherine Hewitt & David Torgerson - 2013 - Journal of Evaluation in Clinical Practice 19 (4):703-707.
Reporting of patient consent in healthcare cluster randomised trials is associated with the type of study interventions and publication characteristics.Andrew McRae, Monica Taljaard, Charles Weijer, Carol Bennett, Zoe Skea, Robert Boruch, Jamie Brehaut, Martin Eccles, Jeremy Grimshaw & Allan Donner - 2013 - Journal of Medical Ethics 39 (2):119-124.

Analytics

Added to PP
2013-11-22

Downloads
21 (#738,221)

6 months
2 (#1,200,611)

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