Important Notice: Our web hosting provider recently started charging us for additional visits, which was unexpected. In response, we're seeking donations. Depending on the situation, we may explore different monetization options for our Community and Expert Contributors. It's crucial to provide more returns for their expertise and offer more Expert Validated Answers or AI Validated Answers. Learn more about our hosting issue here.
The informed consent form is a document that describes a research study, including a clinical trial. It includes the purpose, duration, procedures, risks, benefits, alternative treatments, costs, confidentiality, and study withdrawal information. The informed consent document is reviewed and approved by the IRB.
