What are the key provisions of biomedical law that govern the use of human tissue for research?

Biomedical law in North Carolina governs the use of human tissue for research. Generally, the key principles of this law include informed consent, confidentiality, and regulations regarding the use of tissue samples. Informed consent is when donors provide their consent to the use of their tissue. This consent should be informed and provide details about what the tissue will be used for and any potential risks or benefits associated with the research. Donors should be aware that tissue may be used for future studies and any information collected will be kept confidential. Confidentiality is essential for protecting the privacy of donors and the information collected from their tissue samples. All information should be kept secure and only shared on a need-to-know basis. This means that researchers should avoid sharing information with those who do not have a reason to know about it. Finally, regulations surrounding the use of tissue samples vary by state. In North Carolina, the state law requires researchers to obtain permission from the donor and the right to withdraw consent at any time. The law also prohibits the sale of tissue samples and states that researchers must document the source of the tissue samples. Additionally, the state requires that the results of any research be kept confidential. Overall, the key provisions of biomedical law in North Carolina govern the use of human tissue for research. These include informed consent, confidentiality, and regulations related to the sourcing and use of tissue samples. These provisions are important for protecting the rights of donors, preserving the integrity of research, and ensuring the safety of the tissues used.

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What are the key provisions of biomedical law that govern the use of human tissue for research?

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