What are the legal requirements for patient consent in biomedical research?

In New Hampshire, the legal requirements for patient consent in biomedical research depend on the type of research being conducted. For most types of research, the law requires that the patient or study participant understands the purpose of the research, the procedures involved, the potential risks and benefits, and all other relevant information before they can give consent. This is also referred to as informed consent. The consent should be voluntary and not coerced in any way. In addition, the research should be performed in accordance with accepted medical standards and applicable ethical standards. Furthermore, the patient or study participant should have the option to refuse to participate or withdraw from the research at any time. Minors, pregnant women, and other vulnerable populations are subject to special regulations when it comes to consenting to biomedical research. Generally, parents or guardians must give consent before their children may participate in research. Additionally, special measures may be taken to protect vulnerable populations from potential harms associated with biomedical research. Finally, researchers must always obtain permission from research review boards before conducting any biomedical research. These boards review the research to make sure it meets ethical standards and other legal requirements. In short, the legal requirements for patient consent in biomedical research in New Hampshire include informed consent, voluntary consent, protection for vulnerable populations, and permission from research review boards.

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What are the legal requirements for patient consent in biomedical research?

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