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 ...
On August 15, 2023, the US Food and Drug Administration (FDA) finalized Informed Consent: Guidance for IRBs, Clinical Investigators, and Sponsors (final guidance). This document finalizes, with new ...
The House of Representatives unanimously passed a bipartisan bill that does away with the need for constituents to use a freaking fax machine, or physical mail, to issue "federal consent forms." These ...
NORTH MANKATO, Minn.--(BUSINESS WIRE)--Taylor Healthcare announced it has enhanced its proprietary iMedConsent™ technology solution to help healthcare systems maximize the effectiveness of their ...
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 ...
People who sign consent forms feel more trapped—not more empowered—than those who give consent verbally, according to new ...
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