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Informed consent form Official Title of the study: Assessing the effect of nicotine reduction on ENDS users addiction and exposures NCT number: Not applicable Date of the document: June 17, 2022FIU

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Read the informed consent form carefully to understand all the information provided.

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Fill out all the required fields accurately and truthfully.

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Informed consent form official is needed by individuals who are participating in research studies, clinical trials, medical treatments, or any other activities where their consent is required for participation or treatment.

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What is informed consent form official?

The informed consent form official is a document that outlines the risks and benefits of a particular medical procedure or research study, and it is used to ensure that individuals understand what they are agreeing to before giving their consent.

Who is required to file informed consent form official?

Medical professionals, researchers, or any entity conducting a medical procedure or research study are required to provide and obtain informed consent forms from their patients or participants.

How to fill out informed consent form official?

The informed consent form official should be filled out by providing detailed information about the procedure or study, potential risks and benefits, alternatives, confidentiality, and contact information for questions. The individual must then read and sign the form to indicate their understanding and agreement.

What is the purpose of informed consent form official?

The purpose of the informed consent form official is to ensure that individuals have all necessary information to make an informed decision about participating in a medical procedure or research study, and to protect their rights and well-being.

What information must be reported on informed consent form official?

The informed consent form official must include information about the nature of the procedure or study, potential risks and benefits, any alternative treatments, confidentiality measures, contact information for questions, and space for the individual to give their voluntary consent.

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