What are the legal requirements for conducting experimental treatments?
In New Hampshire, the legal requirements for conducting experimental treatments are outlined in the New Hampshire Right to Try Act. The Act states that patients who have a terminal illness, or an illness that does not respond to standard treatments, can be eligible for experimental treatments. The patient must have received consent from their doctor, and the doctor must have determined that the treatment is reasonable and in the patient’s best interests. The experimental treatment must have received approval from an institutional review board, which is an independent body that reviews the safety, ethics, and efficacy of experimental treatments. Before any experimental treatments can be used on a patient, the physician must also receive written permission from the patient or the patient’s legal guardian. The patient must be informed of all possible risks and benefits of the treatment, and they must provide their informed consent. The patient can choose to revoke their consent at any time. In addition, the experimental treatment must be administered in a hospital or a clinical setting, with the approval of the doctor and the patient. All records must be kept up to date with the patient’s progress, and the patient must be monitored regularly for any adverse effects. Finally, the doctor must be a qualified physician, and must only administer treatments that are approved by the FDA or the New Hampshire Department of Health and Human Services.
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