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So, Andrew, could you walk us through how you conduct a conversation about informed consent with a patient and their family? Right. This is actually of paramount importance because we can never have a patient participate in a study without their clear understanding of everything theyre getting into and that whole process is called informed consent, that theyre making an informed decision on their own, understanding of all the risks and benefits weve talked about of participating in a study. So theres the verbal conversation that goes along with that. But there is actually a written document, sometimes its 20 plus pages long but its very patient friendly and understandable. For patients who may speak a different language, sometimes well make sure that consent form is provided in their native language. Its so important for them to really understand that. And if Im seeing a patient for the first time and proposing a study that they might be eligible for, Ill give them this in
