How does the law regulate the use of digital health records in biomedical research?

In Oregon, biomedical research is regulated by both state and federal law. The use of digital health records is regulated by Oregon’s Health Care Data Privacy Act, which requires that health care providers maintain patient privacy and security when using digital health records. This means that health care providers must protect patient data from unauthorized access, use, or disclosure. The Oregon Health Care Data Privacy Act also requires health care providers to obtain patient consent before sharing data with researchers for biomedical research. Patient consent must be given voluntarily and cannot be coerced. The law also specifies that patients must be informed of the purpose and scope of research the data will be used for. In addition, the Oregon Health Care Data Privacy Act prohibits the sale of digital health information for biomedical research. Furthermore, researchers must obtain patient consent before obtaining access to digital health records, and the records must be used solely for the purpose intended. In summary, Oregon law regulates the use of digital health records in biomedical research through restrictions on the sale of digital health information, ensuring that patient consent is obtained, and protecting patient privacy and security. By following these rules, researchers can ensure that digital health records are used ethically and properly.

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