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
