How does the law regulate the use of digital health records in biomedical research?
In Michigan, the law regulates the use of digital health records in biomedical research by requiring informed consent from research subjects. This means that a researcher must explain the research project to a potential subject and obtain their written consent before any of their data or medical information can be used. Additionally, the researcher must describe the risks, benefits, and other important information associated with the research. To protect the privacy of research subjects, the law also requires the use of secure systems and facilities for storing and transmitting digital health records. This means that all data must be protected against unauthorized access and use. Furthermore, the researcher must take measures to ensure that confidential information is properly regulated and not released without the express consent of the research subjects. The law also requires that the use of digital health records in biomedical research be for legitimate and approved purposes only. This means that any data collected must be used to advance medical knowledge and not for commercial gain or personal gain. Finally, the law requires researchers to properly document their research and disclose any conflicts of interest. This ensures that the research is conducted ethically and that it is done for the greater good rather than for any ulterior motive.
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