How does the law protect information collected through biomedical research?

In Illinois, the law protects information collected through biomedical research in several ways. First, the Health Insurance Portability and Accountability Act (HIPAA) requires researchers to maintain the privacy and security of personally identifiable health information that is collected or used in biomedical studies. Additionally, under the Illinois Human Rights Act, participants must be informed of their rights when participating in such research. They must also be made aware of the risks associated with the research, as well as the availability of other options for care and treatment. Other laws, such as the Illinois Genetic Information Privacy Act, are in place to protect participants from being discriminated against based on any genetic information obtained as part of biomedical research. In addition to these laws, institutional review boards (IRBs) have been established to review and approve biomedical research and ensure that the rights and welfare of human participants are protected. IRBs must review the research protocols of a study, review informed consent documents, and oversee the safety of the participants. Furthermore, the Food and Drug Administration (FDA) also sets guidelines and ensures that biomedical research is conducted in a safe and ethical manner. Overall, the law is in place to ensure that information collected through biomedical research is safely and ethically protected. Participants must be informed of their rights, and research must be conducted in accordance with the guidelines set by the FDA and reviewed by an IRB to ensure the safety and privacy of participants in biomedical research.

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How does the law protect information collected through biomedical research?

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