Literature DB >> 29230696

An Exploration of the Protective Effects of Investigators' Ethical Awareness upon Subjects of Drug Clinical Trials in China.

L Zhang1, X X Huang1, H F Chen2.   

Abstract

Up till now, China has not enacted any legal mechanisms governing certification or supervision for ethics committees. This article analyses deficiencies in the protection of subjects in clinical drug trials under China's current laws and regulations; it emphasizes that investigators, as practitioners who have direct contact with subjects, play significant roles in protecting and safeguarding subjects' rights and interests. The paper compares the status quo in China in this area to that of other countries and discusses ways China might enhance the protection of rights and interests of trial subjects, such as enhancing the ethical awareness of investigators through training, improving laws and regulations, and strengthening the communication between investigators and ethics committees.

Keywords:  China; Ethics committees; Human subjects research; Informed consent; Insurance; Research ethics

Mesh:

Year:  2017        PMID: 29230696     DOI: 10.1007/s11673-017-9826-5

Source DB:  PubMed          Journal:  J Bioeth Inq        ISSN: 1176-7529            Impact factor:   1.352


  18 in total

1.  Clinical trial insurance in a comparative law perspective.

Authors:  Jos Dute
Journal:  Med Law       Date:  2004

2.  Effect of the accountable care act of 2010 on clinical trial insurance coverage.

Authors:  Sheetal M Kircher; Al B Benson; Matthew Farber; Halla S Nimeiri
Journal:  J Clin Oncol       Date:  2011-12-27       Impact factor: 44.544

3.  Fatal trials: clinical trials are killing people.

Authors:  Amit Sengupta
Journal:  Indian J Med Ethics       Date:  2009 Jul-Sep

4.  Profiling cumulative proportional reporting ratios of drug-induced liver injury in the FDA Adverse Event Reporting System (FAERS) database.

Authors:  Allen D Brinker; Jenna Lyndly; Joseph Tonning; David Moeny; Jonathan G Levine; Mark I Avigan
Journal:  Drug Saf       Date:  2013-12       Impact factor: 5.606

5.  Uniform requirements for manuscripts submitted to biomedical journals.

Authors: 
Journal:  N Engl J Med       Date:  1997-01-23       Impact factor: 91.245

6.  Compensation of research-related injuries in the European Union.

Authors:  Miguelangel Ramiro Avilds
Journal:  Eur J Health Law       Date:  2014-12

7.  Volunteer human subjects' understandings of their participation in a biomedical research experiment.

Authors:  Norma Morris; Brian Bàlmer
Journal:  Soc Sci Med       Date:  2005-08-08       Impact factor: 4.634

8.  Recommendations guiding physicians in biomedical research involving human subjects. World Medical Association Declaration of Helsinki.

Authors: 
Journal:  J Med Liban       Date:  1994

Review 9.  [What a surgeon needs to know of the work of a medical ethics committee/institutional review board].

Authors:  N Beck
Journal:  Zentralbl Chir       Date:  2014-03-18       Impact factor: 0.942

Review 10.  A New Ethical Challenge for Institutional Review Boards (IRBs)/Ethics Committees (ECs) in the Assessment of Pediatric Clinical Trials.

Authors:  Klaus Rose; Hans Kummer
Journal:  Children (Basel)       Date:  2015-05-28
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  1 in total

1.  The Power of Knowledge, Responses to Change, and the Gymnastics of Causation.

Authors:  Michael A Ashby; Bronwen Morrell
Journal:  J Bioeth Inq       Date:  2018-03       Impact factor: 1.352

  1 in total

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