Info Sheet

Effective, Ethical Research Through Informed Consent

Translate a protocol document into an understandable form

Obtaining the effective informed consent for individuals participating in a clinical trial is paramount to ethical research. The informed consent form (ICF) outlines for potential research participants the important aspects of the trial, relevant to their decision to participate, which ultimately impacts site enrollment. Oftentimes, potential participants struggle to understand the ICF, complicating their ability to make an informed decision on whether or not they want to proceed. Advarra’s Services for ICF writing ensures compliant, efficient, and easily understandable consent form documentation.

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Time: 1 p.m. ET, 12 p.m. CT, 10 a.m. PT
Duration: 1 hour

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