As mobile devices and online interactions become more prevalent in the healthcare space, digitizing processes such as receiving informed consent from patients will help hospitals and health systems ...
NEW YORK, Oct. 30, 2025 (GLOBE NEWSWIRE) -- Medidata, a Dassault Systèmes brand and leading provider of clinical trial solutions to the life sciences industry, today announced notable advances to ...
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 ...
PHILADELPHIA, April 8, 2021 /PRNewswire/ — Signant Health, the leader in evidence generation for modern clinical trials, announced today expanded electronic informed consent offerings and enhanced ...
Companies Announce Partnership to Improve the Quality and Efficiency of Clinical Trials at the CenterWatch Forum on Optimizing Clinical Research Performance in Boston, MA PRINCETON, N.J., May 20, 2013 ...
In my many years leading participant recruitment in health research, one of the most common questions I’m asked is, “How do you enable eConsent for health research?” Having led recruitment for a large ...
Federal regulations require that researchers obtain legally effective, documented, voluntary informed consent from prospective subjects (or subjects' legally authorized representatives) before ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback