Researchers reported on patient acceptance of an e-consent tool for asynchronous delivery of study information and for receiving consent from patients.

Here are four findings from the updates: 1. Given the increasing concern over the lack of informed patient consent before training and education-related examinations outside of the medically required ...

The Nuremberg Code (1947) and the Declaration of Helsinki (1978) are credited as the origins of informed consent in clinical research. Participants' informed consent is both a legal and ethical ...

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 ...

Please provide your email address to receive an email when new articles are posted on . Researchers conducted a literature review for informed consent with acute ischemic stroke. Decisions should ...

According to a report from AP, hospitals must obtain written consent from patients before subjecting them to pelvic exams and exams of other intimate areas, such as prostate exams, particularly if an ...

Canadian researchers have published new guidelines intended to make consent forms used in clinical research easier for patients to understand. The guidelines describe 75 core elements for consent ...

Health data’s potential can be vertigo-inducing, with seemingly limitless insights available to be mined from data sets old and new. The risks, too, can turn the stomach: faulty and biased algorithms; ...

December 31, 2025 – PRESSADVANTAGE – Language Scientific, a life-science focused translation and localization provider, is drawing attention to the central role that clinical trial translation ...