What are the laws related to the commercialization of reproductive technologies in the United States?

In the United States, commercialization of reproductive technologies is subject to both federal and state law. At the federal level, the Food and Drug Administration (FDA) regulates the medical development and marketing of products related to reproductive technologies, including assisted reproductive technology (ART) such as in-vitro fertilization (IVF). The FDA works closely with the Centers for Disease Control and Prevention (CDC) to ensure the safety of ART services. In addition, the United States Department of Health and Human Services (HHS) regulates the sale and use of human eggs, sperm, and embryos as well as payment for services related to reproductive technologies. HHS also regulates the use of fetal tissue for medical purposes. At the state level, the laws related to the commercialization of reproductive technologies vary. For example, in Washington, surrogacy contracts are recognized and enforced. Washington also prohibits advertising and soliciting payment for the sale of human eggs and sperm. Additionally, Washington has regulations in place to ensure that the identity of the donor is kept confidential. Overall, the laws related to the commercialization of reproductive technologies in the United States aim to protect individuals and ensure the safety of ART services. These laws help to ensure that individuals who are using reproductive technologies or services receive the best care possible.

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