Informed Consent Development Service

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

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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

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

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10 Tips for Writing Compliant Participant Materials

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Learn More About Informed Consent Development

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