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Page 1 of 6Version 9 November 2016Medical University of South Carolina CONSENT TO BE A RESEARCH SUBJECT Multi center, prospective, randomized trial of bronchoscopy with ultrathin bronchoscope and
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Read the informed consent form carefully to understand the purpose, procedures, and risks involved in the research study.
02
Seek clarifications from the researcher or research team if you have any doubts or questions about the study.
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Provide all necessary personal information accurately and honestly.
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Who needs informed consent for researchstate?

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Anyone who is being asked to participate in a research study needs informed consent. This includes individuals who are part of the target population for the study and meet the inclusion criteria set by the researchers.
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Informed consent for researchstate is a process in which participants are fully informed about the research study and voluntarily agree to participate.
Researchers conducting the study are required to file informed consent for researchstate.
To fill out informed consent for researchstate, researchers must include specific information about the study, risks, benefits, and participant rights.
The purpose of informed consent for researchstate is to protect participants' rights, ensure their well-being, and maintain ethical standards in research.
Informed consent for researchstate must include details about the study procedures, purpose, risks, benefits, confidentiality, and contact information for questions or concerns.
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