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ethics committee
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ethics committee

In medicine, review panel made up of both medical and lay people to facilitate medical research in the interests of society, to protect subjects from possible harm due to the research being undertaken, preserve the rights of research subjects, and to provide reassurances to the public on the safety of clinical research. Information provided by researchers should give sufficient detail to enable the ethics committee to evaluate the ethics as well as the scientific merit of the research proposal.

Research involving humans has been governed by protective codes since the 1960s. These codes include those of the World Medical Association (Declaration of Helsinki) and the Medical Research Council in the UK. The development of ethics committees parallels the development of controlled clinical trials of new medicines and surgical procedures since the 1940s and 1950s.



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Whilst a hospital's research ethics committee provides a form of virtual research governance (directing researchers to many documents to assist interpretation of effective research governance), the onus has been largely on the individual researcher to implement research governance as they understand it.
Non-therapeutic research with minors: how do chairpersons of German research ethics committees decide?
They suggest that published research comply with three such protections, these are: seeking research ethics committee approval prior to carrying out research; getting informed consent from participants, and keeping information gathered about participants confidential (Henley and Frank 2006).
 
 
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