Примери коришћења Informed consent на Енглеском и њихови преводи на Српски
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The first of these is informed consent.
Informed consent is necessary for any medical procedure.
Patient information and informed consent.
Other rights: The informed consent document is not a contract;
The documents used to obtain informed consent.
Informed consent is important during any medical procedure.
For all the other cookies your informed consent is required.
Informed consent is important during any medical procedure.
After that, the woman signs an informed consent for the manipulation.
Informed consent is a prerequisite in any medical procedure.
To see how these two frameworks operate,consider informed consent.
Informed consent must be given during all medical procedures.
To see how these two frameworks can differ,consider informed consent.
They can give informed consent for treatment or medical interventions they may need.
However, ethical debate can also arise for studies that have true informed consent.
After signing an informed consent form, the patients were invited for baseline evaluation.
Vaccination is a medical procedure that should include informed consent.
Participants must read andsign the"informed consent" document before joining a trial.
Vaccination is a complex medical intervention andtherefore requires informed consent.
Both frameworks could be used to support informed consent, but for different reasons.
Informed consent is the process of giving clinical trial participants all of the facts about a trial.
For more on medical research before informed consent, see Miller(2014).
The informed consent document explains the risks and potential benefits of taking part in a clinical trial.
First, sometimes asking participants to provide informed consent may increase the risks that they face.
Informed consent includes details about the treatments and tests you may receive and the benefits and risks they may have.
Imagine that you decide to try to receive informed consent from people in the treatment group but not those in the control group.
If informed consent is not possible before a study begins, researchers could(and usually do) debrief participants after the study is over.
Design a hypothetical study where you would have true informed consent from participants, but which you still think would be unethical.
If someone can lie to you or fail to inform you, misrepresent, or withhold information,then there's no such thing as informed consent,” he explains.
Second, sometimes having fully informed consent before the study begins could compromise the scientific value of the study.