Background Electronic approaches are becoming more widely used to obtain informed
consent for research participation. Electronic consent (e-consent) provides an accessible …

Background Informed consent is one of the key elements in biomedical research. The
introduction of electronic informed consent can be a way to overcome many challenges …

Background The increasing integration of digital health tools into care may result in a greater
flow of personal health information (PHI) between patients and providers. Although privacy …

The purpose of this paper is to set guidelines for managing consent and personal data in
ICT businesses taking into account the provisions of the General Data Protection Regulation …

Consent management is a significant function in electronic health information systems as it
allows patients to manage the privacy preferences regarding their health information …

The legal and ethical frameworks that apply in many countries around the world require
service providers to obtain users' agreement to the collection and further processing of their …

User consent is legally and ethically required in any system that collects and uses personal
user data; thus, it is required in internet of things (IoT) systems that depend on users' …

Diabetes is one of the fastest-growing health threats of our times and an urgent public health
issue. In 2015, there were approximately 415 million people diagnosed with diabetes …

Due to national stay-at-home mandates prompted by the COVID-19 pandemic, research
institutions saw a dramatic increase in the number of research informed consents that were …

Current traditional informed e-consent is seen as a one-time agreement for participating in a
research project over a limited period of time. Within the context of Citizen Science, research …