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RESEARCH INFORMED CONSENT Carbon monoxide levels and changes in acute pulmonary function following cigarette use Protocol Number 627260 Sponsor: LB595 Cancer and Smoking Grant Program Principal Investigator:
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How to fill out research informed consent:

01
Read the consent form thoroughly to understand the objectives, procedures, and risks involved in the research.
02
Provide your personal information accurately, including your name, age, gender, and contact details.
03
Carefully review the purpose of the study, ensuring you understand what the researchers aim to achieve.
04
Evaluate the potential benefits and possible risks associated with participating in the research.
05
Seek clarification from the researchers or study coordinator if you have any doubts or concerns about the study.
06
Sign and date the consent form to indicate your voluntary agreement to participate in the research.
07
Consider keeping a copy of the signed consent form for your records.

Who needs research informed consent?

01
Individuals who are approached to participate in research studies.
02
Participants who are asked to provide consent for their involvement in research projects.
03
Research participants who must understand and agree to the purpose, procedures, and potential risks involved in the study.
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Research informed consent is a process where participants are informed about the research study, the potential risks and benefits, and their rights before agreeing to participate.
Researchers conducting a study involving human subjects are required to obtain and file research informed consent.
Research informed consent forms should be filled out by including all necessary information about the study, risks, benefits, and participant rights. Participants should then review and sign the form.
The purpose of research informed consent is to protect participants by ensuring they are fully informed about the study before deciding to participate.
Research informed consent forms should include details about the study purpose, procedures, risks, benefits, confidentiality, and participant rights.
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