eConsent is a tool that can improve the site staff/patient discussion. Informed consent forms (ICFs) have become increasingly complex, technical and more difficult for patients to understand clinical research objectives.

While informed consent form (ICF) signatures traditionally have been collected on paper at a physical site, today’s digital approach — electronic consent (eConsent) — offers more than high-tech signature collection.

This guidance provides recommendations on the use of electronic systems and processes that may employ multiple electronic media to obtain informed consent for both HHS-regulated human subject...

Trying to access eConsent? Make sure your device is connected to CHLA’s internal network by following the instructions at:

What is the eConsent Toolkit? The eConsent Toolkit presented here provides samples of the tools, resources, and educational materials used in the project. They represent just one method of enabling patient education and engagement for meaningful consent.

Veeva eConsent provides a digital way to consent clinical trial participants in-person or remotely. Break free from legacy tools and cumbersome paper documents. Give your patients access to a modern digital consent experience that fits into their daily lives.

What is eConsent? eConsent involves using electronic devices (e.g., computer, tablet, phone) to obtain consent from a potential participant or legally authorized representative. The benefits of eConsent include: Enabling.

Dec 4, 2023 · Electronic consent (eConsent) is a method of obtaining agreement from an individual. It’s also known as electronic informed consent (eIC). For example, medical researchers must obtain consent for trials of new therapeutic drugs or devices.

eConsent is the digital process of obtaining informed consent from participants in clinical research. It involves providing comprehensive, user-friendly information about the trial electronically, often through videos, images, or interactive content.

eConsent reduces paperwork for clinical staff, enhancing accuracy and efficiency. Sponsors gain real-time participant consent data, supporting study management and regulatory processes. eConsent helps cut down on paperwork during monitoring visits, audits, and inspections.