On the other hand, eICs also raise privacy and secure data storage regulation compliance concerns. The eIC, if properly implemented, will be of significant benefit to institutional review boards (IRBs ...
VALENCIA, Calif., Oct. 24, 2012 /PRNewswire/ -- Sanguine BioSciences, a biotechnology company providing transparency to patients in biomedical research, has announced its plans to deploy its @Home, ...
Obtaining informed consent is a basic ethical obligation and a legal requirement for researchers. This requirement is founded on the principle of respect for persons. Potential participants must be ...
Joel A Friedlander, Greg S Loeben, Patricia K Finnegan, Anita E Puma, Xuemei Zhang, Edwin F de Zoeten, David A Piccoli and Petar Mamula Objectives To evaluate the adequacy of paediatric informed ...
Nine years after the draft version was published, the Food and Drug Administration (FDA) has finalized its guidance on informed consent for sponsors, institutions, IRBs, and investigators. The final ...
One of the major obstacles for researchers when deciding whether to adopt an eConsent approach within their study has been a lack of understanding surrounding regulatory support. While many would ...
Federal regulations require that researchers obtain legally effective, documented, voluntary informed consent from prospective subjects (or subjects' legally authorized representatives) before ...
New study* reveals greater comprehension and personal engagement with enhanced e-consent PALO ALTO, Calif., January 31, 2024--(BUSINESS WIRE)--Medable Inc., the leading technology provider for modern ...
In the present world, consent is a significant element in all aspects of healthcare dispensation. Its legal and ethical necessity stems from the basic right of self-determination. In surgical practice ...
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