Informed Consent Development Service


Ensure your clinical trial documentation is compliant while making study activation more efficient.

Contact Us

Technology Products

Failing to craft a comprehensive, easy-to-read informed consent form can result in uninformed participants and lower trial retention rates.

Advarra’s experts have the ability to translate a protocol document into a compliant and understandable consent document, allowing sites to enroll participants onto protocols quicker.

Our services include:

Informed Consent: 6 Approaches to Increase Participant Comprehension

Download the white paper

Informed Consent: When, Why, and How It’s Obtained

Read the blog

10 Tips for Writing Compliant Participant Materials

Read the white paper

Learn More About Informed Consent Development

Contact Us