There are several types of informed consent, those in the private physician/dentist office and those that protects human subjects

Types of Informed Consent

 

  1. There are several types of informed consent, those in the private physician/dentist office and those that protects human subjects. Describe the difference between informed consent that is obtained at a private physician’s office as compared to one obtained before undertaking a research study
  2. Where did the concept of informed consent originate? What is the purpose of obtaining informed consent? Is there a right or a wrong way?
  3. Why is the protection of human subjects important training for all health care personnel to complete

 

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The informed consent from the private physician’s office is meant to acquire permission for subjecting the patient to a diagnostic or treatment procedure. In this case, the patient is informed about the risks or dangers involved in the process. In most cases, the physicians obtain this consent to help the patients. On the other hand, the consent obtained from the use of human subjects in research is permission acquired by the researchers. In most cases, the researchers are the beneficiaries of the study (Kakar et al., 2014).  Additionally, the document used in writing informed consent of research is much bigger than that used is a private doctor’s office as the latter is usually one page or less. In the research, the informed consent is approved by IRB, whereas the hospital approves the informed consent during a medical procedure on a patient……………

APA 396 words

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