Get your free white paper: 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.

You learn:

  • What electronic informed consent is
  • The regulatory requirements of using electronic informed consent technology
  • The benefits of electronic informed consent to clinical researchers