Develop an informed consent for a research study titled”the Impact of Permissive Underfeeding versus Target Enteral Feeding on Mortality and Morbidity in Adult Critically Ill Patients: A Multicenter Randomized Controlled Trial” that has to be taken from prospective subjects to participate in this study.
In order for you to develop this consent I need you to follow the attached guidelines titled(documentation of consent to participate in a research study & title 21 sub part B documents) and to refer to the two power points provided(informed consent process and informed consent elements)
