Those who conduct research have a duty to act in an ethical manner that does not exploit
participants in research. Canada's Health Minister Rona Ambrose has recently breached …

© 2012 Canadian Medical Association or its licensors CMAJ, April 3, 2012, 184 (6) 657
government or regulatory approval of new drugs and devices is sought. Again, this differs …

Abstract Is Institutional Review Board (IRB) approval and a rigorous informed consent
process enough? It is our view that this is no longer the case. Conventional research ethics …

In research ethics there is a canon regarding what ethical rules ought to be followed by
investigators vis‐à‐vis their treatment of subjects and a canon regarding what fundamental …

Clinical trials in developing coun-tries done by US researchers or sponsored by US
agencies should be limited to research that is “responsive to the needs” of the host country …

The temptation in clinical research to sacrifice the interests, the health, and sometimes even
the lives of research subjects to the advancement of the interests of science and society, and …

Human research must respect most rigorous ethical standards to protect both the
investigators and subjects. Codes of ethical practice relevant to such research are subjected …

380 stronger protections for human research subjects in 2000.“There's more recognition that
research participants aren't just individuals, they are part of families and communities …

There has been a growing concern over establishing norms that ensure the ethically
acceptable and scientifically sound conduct of clinical trials. Among the leading norms …

M edical research has long been performed on human volunteers who risk their own well-
being for society's greater good. Safeguarding human rights and upholding ethical …