Clinical trial patient consent form

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Study of Isatuximab, bortezomib, lenalidomide, dexamethasone in multiple myeloma. Collection of Tissue Samples for Cancer Research. Natural History of Familial Carcinoid Tumor. Sheffield, England, United Kingdom. Parexel International Corporation. Argentina - Any Region - Home Based. Germany - Any Region - Home Based.

Shanghai, Shanghai Municipality, China. Shrewsbury, MA, US, It looks like you're using Internet Explorer 11 or older. This website works best with modern browsers such as the latest versions of Chrome, Firefox, Safari, and Edge. If you continue with this browser, you may see unexpected results.

Introduction blah blah blah. Clinical trials are used to answer questions such as:. How should the product be used? While research subjects may get personal treatment benefit from participating in a clinical trial, they must understand that they:. To make an informed decision about whether to participate or not in a clinical trial, people need to be informed about:. This information is provided to potential participants through the informed consent process. Informed consent means that the purpose of the research is explained to them, including what their role would be and how the trial will work.

A central part of the informed consent process is the informed consent document. The Food and Drug Administration FDA does not dictate the specific language required for the informed consent document, but does require certain basic elements of consent be included. A description of all the procedures that will be completed during enrollment on the clinical trial.

Any possible discomforts e.