this is a two part discussion
- 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
- Where did the concept of informed consent originate? What is the purpose of obtaining informed consent? Is there a right or a wrong way?
- Why is the protection of human subjects important training for all health care personnel to complete
Solution Preview
Types of Informed Consent
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.
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