Research ethics approval and discrimination
نویسندگان
چکیده
منابع مشابه
Need for ethics approval and patient consent in clinical research.
A key principle in clinical research is the need to obtain approval from a Research Ethics Committee before commencing a study, and then to obtain consent from each subject enrolled into the study. This tenet is highlighted in the Helsinki Declaration and reinforced in subsequent principles such as Good Clinical Practice/International Committee on Harmonisation. However, not all clinical studie...
متن کاملEthics approval: responsibilities of journal editors, authors and research ethics committees
Meaningful progress of medicine depends on research that must ultimately involve human subjects. Obtaining ethical approval therefore, especially in medical sciences, should be a moral reflex for researchers. This unfortunately is not the case, with numerous researchers bypassing the ethics approval procedure, or simply unaware of its importance. Good research involves risks taken by research p...
متن کاملResearch ethics approval for human and animal experimentation: consequences of failing to obtain approval--including legal and professional liability.
56 ** Tracey Tremayne-Lloyd, LLB, BA, is a Health Law Lawyer (Partner) a ** Dr. Gary Srebrolow, LLB, DDS, BSc, is a Health Law Lawyer at Gard The authors wish to acknowledge the assistance of Angela Chu, Studen of Ontario (CCO), and criminal law to protect test subjects and ensure that animal and other human experiments are conducted in a safe and socially responsible manner. REBs have the powe...
متن کاملResponses of local research ethics committees to a study with approval from a multicentre research ethics committee.
itself. The multicentre research ethics committee system was set up to deal with such procedural difficulties. Improvements in the system have occurred. However, local research ethics committees have been reluctant to abandon their autonomy sufficiently to allow efficient functioning of this system, and this has been identified as a potential reason for continuing concerns about the new system....
متن کاملResearch and the Approval Process ∗
An agent (such a pharmaceutical company) sequentially collects information (through clinical trials) to obtain a principal’s (the FDA) approval (to introduce a new drug). Principal and agent both pay the cost of information, but they derive different payoffs from adoption. We characterize how the principal can benefit from commitment to an approval standard and how the commitment solution compa...
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ژورنال
عنوان ژورنال: The Psychiatric Bulletin
سال: 2014
ISSN: 2053-4868,2053-4876
DOI: 10.1192/pb.38.2.89