Research on rare diagnoses and the development of precision medicine depend on patients being able to share their health data in a secure and ethical manner. The research study, published in ...

In today’s digital world, we often desire to have people consent to documents by merely pasting an image of a signature into a document, clicking a virtual button on a web site or mobile phone, or ...

Care at Your Fingertips: Codesign, Development, and Evaluation of the Oncology Hub App for Remote Symptom Management in Pediatric Oncology We surveyed institutions in the National Comprehensive Cancer ...

Upon receiving information, patients were able to give preliminary consent on a survey form, and this allowed collection of a first blood sample and further communication. The use of an asynchronous ...

CHARLESTON, S.C. (WCIV) — A new bipartisan bill, the Electronic Consent Accountability Act, seeks to modernize how Americans access their federal records by bringing transparency and accountability to ...

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 ...