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Supplementary material BMJ OpenSupplement 2: Study information sheet and informed consentINFORMATION ABOUT THE STUDY You have shown your interest in participating in a scientific study of University
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To fill out supplement 2 study information, follow these steps:
02
Start by providing your personal information, such as your full name, date of birth, and contact details.
03
Next, provide details about your educational background, including the schools or universities you attended and the degrees or qualifications you obtained.
04
Provide information about your previous study experiences, such as the duration of your studies, the areas of study, and any research work or projects you completed.
05
Include any additional information relevant to your study experience, such as internships or extracurricular activities related to your field of study.
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Finally, review the filled information for accuracy and completeness before submitting the supplement 2 study information form.

Who needs supplement 2 study information?

01
Supplement 2 study information is required by individuals who are applying for certain educational programs or scholarships. This information is typically requested by educational institutions or scholarship committees to assess the applicant's academic background and suitability for the program or scholarship.
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Supplement 2 study information pertains to additional data and findings that need to be reported by researchers or institutions conducting specific studies, usually related to regulatory compliance.
Researchers, institutions, or sponsors conducting studies that fall under certain regulatory guidelines are required to file supplement 2 study information.
To fill out supplement 2 study information, individuals should complete the designated form, ensuring all relevant data and findings are accurately recorded and submit it according to the provided guidelines.
The purpose of supplement 2 study information is to provide additional context, data, and results about a study that may be pertinent for regulatory review, compliance, or research integrity.
Information that must be reported includes detailed study results, methodologies used, participant data, any adverse events, and how the data aligns with regulatory requirements.
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