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Study #: S2101226 Version date: 2022.01.27Page 1 of 17[Insert logo here]l NYU Lang one\'... Healthline 3 Research Participant Informed Consent Fertile of Study:NIH RECOVER: A Multisite Observational
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Start by gathering all the necessary information about the level 3 research participant form.
02
Fill out the personal details of the participant such as name, age, gender, contact information, etc.
03
Provide relevant demographic information including race, ethnicity, education level, occupation, etc.
04
Specify the research study details that the participant will be involved in, including the purpose, methodology, and any potential risks or benefits.
05
Document any medical or health-related details that are required for the study.
06
Include any consent forms or agreements that the participant needs to sign.
07
Double-check the filled-in form for any errors or missing information.
08
Submit the completed level 3 research participant form to the appropriate department or research organization.

Who needs level 3 research participant?

01
Researchers conducting advanced studies and experiments often require level 3 research participants.
02
Institutes or organizations involved in scientific research and development
03
Academic institutions conducting research projects or doctoral studies
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A level 3 research participant refers to an individual or entity that is involved in research activities requiring a higher level of regulatory oversight and data reporting compared to level 1 and level 2 participants.
Individuals or entities conducting research that meets specific criteria for level 3 oversight, usually involving sensitive data or higher potential risks, are required to file as level 3 research participants.
To fill out the level 3 research participant form, you must provide detailed information regarding the research project, including participant data, methodology, potential risks, and compliance with ethical standards.
The purpose of classifying participants at level 3 is to ensure comprehensive monitoring and reporting on research activities that involve complex issues, thereby enhancing ethical oversight and participant safety.
Information that must be reported includes the participant's identity, research objectives, methodology, risk assessments, data handling procedures, ethical compliance, and any adverse events.
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