In her Health Affairs Blog post last fall, Sharon Brownlee lamented how frequently patients agree to treatments that they know little about. In the United States and elsewhere, clinicians have a clear ...

Informed consent has been defined as "an individual's autonomous authorization of a medical intervention or of participation in research". [1] In professional and legal regulations it is widely ...

While many people indicate “I have read and agree to the terms and conditions”, very few actually take the time to read through everything to truly understand the small print. One journalist estimates ...

The IRB determines, for each protocol it reviews, which of the following elements and disclosures must be included in the informed consent process. Investigators can avoid delay in the review process ...

When you shop through retailer links on our site, we may earn affiliate commissions. 100% of the fees we collect are used to support our nonprofit mission. Learn more. A fter seeing an ear, nose, and ...

Over the past 50 years, the informed consent process has become increasingly regulated and standardized, while the challenges remain persistent and hard to overcome. 8 Consent forms are increasingly ...

The use of deception or incomplete disclosure limits the subject's ability to make a fully informed decision of whether to participate in the research — one of the essential ethical concerns in human ...

What is informed birth consent? Here's why it's vital. (Getty Images) Consent in the medical field is vital to ensuring a patient’s comfort and safety. Some people, however, are sounding the alarm ...

Most lawsuits related to botulinum toxin result from “unexpected harm or injury, like a poor cosmetic outcome or complication ...

Journal of Empirical Research on Human Research Ethics: An International Journal, Vol. 14, No. 4 (October 2019), pp. 307-317 (11 pages) There is limited literature on the opinions and perspectives of ...

Informed consent is an agreement between the investigators and the research participants. A signed informed consent form notifies potential research participants of their obligations and rights, and ...