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Misti Ault Anderson: Hello, everyone, and welcome to our session today on Simplifying Informed Consent. My name is Misti Ault Anderson, and I am here with my colleague, Yvonne Lau. We both work in the Division of Education and Development in the HHS Office for Human Research Protections. And we are looking forward to talking with you today about the informed consent process, the new requirements and how to use these to get a really meaningful informed consent in a more simplified manner to make it easier for you and for your research participants to understand and join your study. So thank you for joining us today. This session is scheduled for an hour and 45 minutes. We will talk for probably 75 to 90 minutes of that, and then well be opening it up for questions. If you have questions that youd like to submit for us to answer, please enter them into the Q and A portion of the Zoom so that we can address them all through the Q and A as opposed to the chat. So again, please use the Q