Are there any special considerations regarding the regulation of human genetic engineering?
In Michigan, any special considerations regarding the regulation of human genetic engineering are based on the Michigan Medical Policy-Making Act of 1978 and the Michigan Public Health Code of 1978. Under these rules, any research, development, testing, or use of genetic engineering related to the human genome must be reviewed and approved by the Michigan Department of Health and Human Services. The Michigan Department of Health and Human Services must review and approve any proposed clinical trials related to genetic engineering before they can be allowed to proceed. This review must consider the safety of the patient, the medical need of the patient, and the benefits to society. Additionally, any genetic engineering related to human tissue or fluids must include regulations to protect the privacy of the person involved. Researchers who are conducting human genetic engineering must also adhere to ethical guidelines and laws regarding clinical trials. This includes laws forbidding any experimentation on minors, the mentally ill, or prisoners. In addition, researchers must practice informed consent procedures, which include giving the person involved with information about the study, the risks involved, and the procedures that will be used. These ethical guidelines are important in ensuring that all human genetic engineering is conducted with the highest standards of safety and respect for the person involved.
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