A Patient Informed Consent Form is a voluntary agreement between a doctor or a medical organization to participate in research. Although as simple as it may seem, this is not just an ordinary consent form. An Informed Consent Form intends to orient the potential participant about the overview of which he or she is being recruited for as well as other information about the program, any expectations, the procedures, among others. Having an informed consent lets the parties in the agreement overcome some of the legal hurdles in conducting studies or trials from patients. Thus, the patient's legal rights are not intruded or encroached upon by the researchers or doctors.