Are there special precautions for use of experimental drugs and devices?
Yes. In addition to obtaining the Food and Drug Administration’s approval to proceed with research involving a new drug or device, health care providers also must obtain review and approval by an Institutional Review Board (IRB). The IRB is a group of individuals who assure the protection of patients’ rights and welfare. If the IRB determines that the risks of the research outweigh the benefits, it can modify or disapprove the research. The IRB also ensures that information given to people who are deciding whether or not to participate in the research is thorough and accurate. How do I arrange to donate body parts after my death? You may give all or any part of your body for transplant, therapy, medical or dental education, or research by signing the statement on your driver’s license or by stating these wishes in your will or in a separate document. If you later change your mind, you may amend or revoke your decision by signing a statement of amendment or revocation, verbally amending
