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Center Number: Study Number: Patient Identification Number for this trial:Additional CONSENT FORM for control individuals (attached to main consent form) Title of Project: Irish Rare Kidney Disease
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Start by reading the instructions provided with the additional consent form.
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Provide all the required personal information, such as your name, address, and contact details.
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Fill out the consent form completely and accurately, ensuring that all the necessary fields are completed.
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Who needs additional consent form for?

01
The additional consent form is typically required for individuals who need to provide consent for specific purposes, such as medical procedures, research studies, legal agreements, or parental consent for minors.
02
The specific requirements may vary depending on the organization or situation, so it's essential to check the guidelines or ask the relevant authority for clarification.
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The additional consent form is used to obtain permission from participants for various purposes, such as data collection or the use of personal information.
Individuals or organizations that are conducting research or activities involving personal data collection and require consent from participants are required to file the additional consent form.
To fill out the additional consent form, clearly provide detailed information about the purpose of the study, the procedures involved, risks, benefits, and obtain signatures from all participants acknowledging their consent.
The purpose of the additional consent form is to ensure that participants are fully informed about the activities they are consenting to and to safeguard their personal rights and data.
The additional consent form must report information such as the nature of the study, the use of data collected, potential risks, benefits, and the rights of participants.
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