The process of obtaining informed consent for clinical trials is tightly regulated; complications arise in circumstances when consent may be waived, or when needed from vulnerable populations http://ow.ly/rEMe30j5MVq
Informed consent of the participant in medical research is the expression of the recognition of the ...
Background: Informed consent, a critical enabler of clinical research, depends on the provision of r...
Informed consent is important: in research, it allows subjects to make an informed and voluntary cho...
The process of obtaining informed consent for clinical trials is tightly regulated; complications ar...
Informed and voluntary consent are important aspects when conducting human research and is an area t...
Worldwide, the goal of clinical research is to develop knowledge that improves human health or augme...
Background: Ethical problems most often arise in research. One of the most important ethical rules g...
Informed consent refers to the process of giving information, discussing and obtaining permission of...
Informed consent for medical research is an essential, but challenging, process to assure the protec...
Informed consent is a process in which a human subject who is to participate in research needs to gi...
Obtaining informed consent is a prerequisite for a subject's participation in a research project. In...
AbstractEthically sound clinical research requires that prospective study participants provide volun...
A study was conducted among participants in an antiretroviral therapy (ART) clinical trial to determ...
Informed consent requires that potential clinical trial subjects be fully-informed and capable of ma...
The current doctrine of informed consent falls far short of its potential to serve as a valuable saf...
Informed consent of the participant in medical research is the expression of the recognition of the ...
Background: Informed consent, a critical enabler of clinical research, depends on the provision of r...
Informed consent is important: in research, it allows subjects to make an informed and voluntary cho...
The process of obtaining informed consent for clinical trials is tightly regulated; complications ar...
Informed and voluntary consent are important aspects when conducting human research and is an area t...
Worldwide, the goal of clinical research is to develop knowledge that improves human health or augme...
Background: Ethical problems most often arise in research. One of the most important ethical rules g...
Informed consent refers to the process of giving information, discussing and obtaining permission of...
Informed consent for medical research is an essential, but challenging, process to assure the protec...
Informed consent is a process in which a human subject who is to participate in research needs to gi...
Obtaining informed consent is a prerequisite for a subject's participation in a research project. In...
AbstractEthically sound clinical research requires that prospective study participants provide volun...
A study was conducted among participants in an antiretroviral therapy (ART) clinical trial to determ...
Informed consent requires that potential clinical trial subjects be fully-informed and capable of ma...
The current doctrine of informed consent falls far short of its potential to serve as a valuable saf...
Informed consent of the participant in medical research is the expression of the recognition of the ...
Background: Informed consent, a critical enabler of clinical research, depends on the provision of r...
Informed consent is important: in research, it allows subjects to make an informed and voluntary cho...
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