The current doctrine of informed consent falls far short of its potential to serve as a valuable safeguard for human research subjects. Instead of providing a channel of communication between physician and subject, informed consent is a lifeless entity responsible for a large portion of the misunderstanding existing between these parties. Acknowledging risk perception principles may help transform the informed consent process into an effective communication of health risks
For several decades Clinical trials are a "back-bone" of new drug development. Even if Ethical codic...
The process of informed consent is an ethical mandate for all clinical trials. The principles of eth...
Practice and law around informed consent in healthcare have undergone a revolution for the better ov...
The current doctrine of informed consent falls far short of its potential to serve as a valuable saf...
“Full disclosure is a necessary precondition to free choice. Accordingly, subjects who do not unders...
Informed consent is important: in research, it allows subjects to make an informed and voluntary cho...
The current ethical and regulatory framework for research is often charged with burdening investigat...
Worldwide, the goal of clinical research is to develop knowledge that improves human health or augme...
Informed consent has traditionally focused on treatment-related issues. However, since the mid-1990s...
The doctrine of informed consent, defined as respect for autonomy, is the tool used to govern the re...
The standard account of the (Kahneman and Tversky, 1979) is that attitude toward risk changes across...
The traditional process for obtaining informed consent from potential clinical trial subjects is tim...
Although the principle of informed consent is well established and its importance widely acknowledge...
Informed consent requires that potential clinical trial subjects be fully-informed and capable of ma...
Informed consent is a widely acknowledged ethical principle that plays a crucial role, both in resea...
For several decades Clinical trials are a "back-bone" of new drug development. Even if Ethical codic...
The process of informed consent is an ethical mandate for all clinical trials. The principles of eth...
Practice and law around informed consent in healthcare have undergone a revolution for the better ov...
The current doctrine of informed consent falls far short of its potential to serve as a valuable saf...
“Full disclosure is a necessary precondition to free choice. Accordingly, subjects who do not unders...
Informed consent is important: in research, it allows subjects to make an informed and voluntary cho...
The current ethical and regulatory framework for research is often charged with burdening investigat...
Worldwide, the goal of clinical research is to develop knowledge that improves human health or augme...
Informed consent has traditionally focused on treatment-related issues. However, since the mid-1990s...
The doctrine of informed consent, defined as respect for autonomy, is the tool used to govern the re...
The standard account of the (Kahneman and Tversky, 1979) is that attitude toward risk changes across...
The traditional process for obtaining informed consent from potential clinical trial subjects is tim...
Although the principle of informed consent is well established and its importance widely acknowledge...
Informed consent requires that potential clinical trial subjects be fully-informed and capable of ma...
Informed consent is a widely acknowledged ethical principle that plays a crucial role, both in resea...
For several decades Clinical trials are a "back-bone" of new drug development. Even if Ethical codic...
The process of informed consent is an ethical mandate for all clinical trials. The principles of eth...
Practice and law around informed consent in healthcare have undergone a revolution for the better ov...