What legal protections are available to those involved in clinical trials?

In Kansas, legal protections are available to those involved in clinical trials. According to the Kansas Biomedical Research Act, all research involving human participants requires approval from an Institutional Review Board (IRB). This board is responsible for ensuring that the safety of the participants in the study is protected. Participants must also provide informed consent before participating in any study, which means they are aware of the risks associated with taking part in the study and the potential benefits they may receive. The Kansas Biomedical Research Act also requires that all participants be provided with a patient bill of rights. This includes the right to access their health records, the right to privacy, the right to have their questions answered, the right to be informed about any potential risks or side effects that may occur, and the right to withdraw from the study at any time. Clinical trials are also governed by the federal Common Rule, which provides additional legal protections for study participants. These include the right to be informed about the risks of the study and any potential benefits before making a decision to participate; the right to be informed if there is any new information discovered during the study; and the right to discontinue participating in the study if desired. In addition, study participants may also be eligible for compensation if they are injured due to participating in the study. This may include medical costs and lost wages. It is important for those participating in clinical trials to know and understand their rights and what legal protections are available to them.

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What legal protections are available to those involved in clinical trials?

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