What is the legal framework for medical research?

In South Carolina, medical research is legal and regulated by the South Carolina Medical Research Act. This act sets the guidelines for conducting medical research by individuals, organizations and government entities and regulates the protection of human subjects of medical research. It also sets forth rules relating to informed consent, privacy, and confidentiality of any data collected during the course of medical research. The Medical Research Act defines the legal powers and duties of the Department of Health and Environmental Control (DHEC) through the South Carolina Medical Research Commission, which is responsible for monitoring adherence to the act. It sets out the criteria for research institutes and outlines the procedures for conducting medical research. It also provides for the approval of new drugs and devices for medical research purposes and requires drug and device manufacturers to report any adverse effects resulting from the use of their products. The Medical Research Act also provides for the regulation of research involving human subjects. This includes guidelines relating to the informed consent of participants, privacy and confidentiality of medical information, and ethical guidelines for the conduct of research. It also requires all research involving human subjects to be reviewed and approved by a research ethics committee. The legal framework for medical research in South Carolina is designed to ensure that research is conducted safely and ethically, while still protecting the rights of individuals involved. It provides a framework for regulating medical research while maximizing the benefits obtained.

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What is the legal framework for medical research?

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