What are the legal requirements for sharing information obtained through biomedical research?

Biomedical research generates a lot of data and information that can be shared with the public. In New Hampshire, there are laws that govern how this information can be shared. In New Hampshire, the Release of Information from the New Hampshire Decedents Studies (NHDS) Law determines how information can be shared from individuals who have donated their bodies for biomedical research. There are specific requirements covered under the NHDS law that must be followed. Those requirements include providing clear and direct consent for use of the information. A donor must provide written authorization for the release of information, and the donor must be notified of the use of the information. In addition, the donor must provide consent for the release of any materials related to their donation, such as tissue samples, and must be notified of any use of those materials. The sharing of data from biomedical research must also follow New Hampshire’s Human Research Protection Program. This Program requires that researchers provide proof of informed consent from all research participants. It also requires that researchers keep confidential any identifying information from research participants. In summary, in New Hampshire, legal requirements for sharing information obtained through biomedical research include obtaining clear and direct consent from all donors, providing researchers with proof of informed consent from research participants, and keeping confidential any identifying information from research participants.

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What are the legal requirements for sharing information obtained through biomedical research?

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