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There has been an increased focus over the past couple of years on patient rights, resulting in a renewed emphasis on informed consent by healthcare regulators, such as The Joint Commission. This ...
Informed consent is a process that’s required for most medical procedures. However, there’s often confusion about what informed consent is, what it means, and when it’s needed. In a healthcare setting ...
Thank you for reminding the research and scholarly community of the fundamental importance of striving to obtain each subject’s true informed consent prior to her or his participation in research ...
HIV testing must be voluntary. Patients must know that testing is planned and be informed that they will be tested unless they decline (“opt out”). The patient should be provided information about HIV ...
Please provide your email address to receive an email when new articles are posted on . Informed consent forms for interventional oncology clinical trials are often lengthy and written at too high of ...
A lot has been written about ensuring that the language of informed consent forms is at a level that is easily understandable, and for good reason. The Food and Drug Administration requires all ...
The informed consent model of care is based on providing accurate and in-context information so that you can make the best decision about your healthcare plan. When people talk about options for ...
"If only the doctor had warned me of this terrible complication, I never would have agreed to his treatment." When a patient has a poor outcome, that statement is typically the basis for a malpractice ...