---
title: Electronic Informed Consent for Clinical Investigations
description: "white paper: Electronic Informed Consent for Clinical Investigations - Using Electronic informed consent (eIC) correctly in a variety of research applications."
image: https://www.thefdagroup.com/hubfs/Images/Covers/fda-WP-ElectronicInformedConsent-Cover.jpg
---

| ![](https://www.thefdagroup.com/hubfs/Images/Covers/fda-WP-ElectronicInformedConsent-Cover.jpg) | Get our free guide # Electronic Informed Consent for Clinical Investigations  Using Electronic informed consent (eIC) correctly in a variety of research applications. Electronic informed consent (eIC) offers valuable benefits for those documenting the progress of clinical research, specifically as it relates to managing informed consent records from subjects. In this guide, we’ve laid out the basics of eIC, the advantages this technology offers clinical researchers, and the regulatory requirements for eIC programs in the United States. **What you'll find inside:** - What electronic informed consent is - The regulatory requirements of using electronic informed consent technology - The benefits of electronic informed consent to clinical researchers [Get my free guide »](https://www.thefdagroup.com/informed-electronic-consent-for-clinical-investigations#) |
| --- | --- |
| [![FDA logo](https://www.thefdagroup.com/hubfs/template_2019/img/logo.svg)](https://www.thefdagroup.com/) The FDA Group, LLC will not be liable for any errors or omissions in this information nor for the availability of this information. The owner will not be liable for any losses, injuries, or damages from the display or use of this information. [Privacy Policy](https://www.iubenda.com/privacy-policy/7819312) |  |

### Get the Guide

![](https://dc.ads.linkedin.com/collect/?pid=19851&fmt=gif)