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APPROVED Dec 11, 2014 WIRE Research Subject Information and Consent Document TITLE: Open Humans: Public Data Sharing PROTOCOL NO.: None WIRE Protocol #20141970 Sponsors: PersonalGenomes.org INVESTIGATOR:
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How to fill out research subject information and:

01
Start by gathering all necessary information about the research subject. This may include their name, age, gender, contact details, and any relevant background information.
02
Ensure accuracy and completeness of the gathered information by verifying it with the research subject themselves or through other reliable sources.
03
Use a standardized and well-structured form to record the research subject information. This will make it easier to organize and analyze the data later on.
04
Clearly label each field or section in the form to indicate the type of information required. For example, separate sections for personal details, medical history, or previous participation in research studies.
05
Provide clear instructions to the research subjects on how to accurately complete each section of the form. This could be done through written instructions, in-person guidance, or both.
06
Keep the research subject information confidential and secure. Ensure that it is stored in a secure location or database, accessible only to authorized personnel.

Who needs research subject information and:

01
Researchers: Research subject information is crucial for researchers to understand and analyze the characteristics and demographics of their study participants. It helps them identify patterns, trends, or potential biases within the data.
02
Ethical Review Boards: Ethical review boards or committees may require access to research subject information to ensure that ethical guidelines and regulations are being followed. They use this information when evaluating research proposals to ensure the protection of human subjects.
03
Funding Agencies: Funding agencies may request research subject information as part of their grant evaluation process. This information helps them determine the scientific merit, relevance, and potential impact of the proposed research.
04
Institutional Review Boards (IRBs): IRBs are responsible for reviewing and approving research studies involving human subjects. They need access to research subject information to assess the risks, benefits, and ethical considerations involved in the study.
05
Regulatory Bodies: Regulatory bodies, such as government agencies, may require research subject information to monitor and ensure compliance with laws and regulations related to research involving human participants.
Overall, research subject information is essential for the proper conduct of research studies, ensuring ethical standards are upheld, and enabling accurate analysis and interpretation of data.
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Research subject information refers to data and details about the individuals who are participating in a research study.
Researchers or research institutions are required to file research subject information.
Research subject information can be filled out by providing accurate and detailed information about each research participant.
The purpose of research subject information is to ensure transparency, confidentiality, and compliance with ethical standards in research studies.
Research subject information typically includes details such as age, gender, medical history, consent forms, and any other relevant data.
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