Making Your Consent Forms Readable: The Why and the How
Presented by Wendy Tate
Informed consent is one of the pillars of ethical clinical research. Despite this, the majority of consent forms are written using language that is beyond the reading comprehension of the target population. In this complimentary webinar, Wendy Tate will discuss the HHS and FDA requirements regarding the content of an informed consent form as well as provide tips for making your consent form more understandable to your study population.
Previously recorded: June 21, 2016
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