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Finis vaccine trial Study protocol: 111442 (10PNPDDIT043) Informed consent form CONFIDENTIAL INFORMATION SHEET AND CONSENT FORM FOR PARENT / GUARDIAN Study title and number: 111442 (10PNPDDIT043)
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How to fill out study information and consent:

01
Begin by carefully reading through the study information and consent form. Make sure you understand the purpose and objectives of the study, as well as any potential risks or benefits involved.
02
Provide your personal information accurately and honestly. This may include your name, age, gender, contact information, and any other relevant details required by the study.
03
Date and sign the consent form. By doing so, you acknowledge that you have understood the information provided and voluntarily agree to participate in the study. This is an important step to ensure that your participation is fully informed and that you have given your consent willingly.
04
If you have any questions or concerns about the study or the consent form, don't hesitate to seek clarification from the researchers or study coordinators. It is crucial for you to have all the necessary information before making a decision to participate.

Who needs study information and consent?

01
Individuals who are considering participating in a research study or clinical trial need study information and consent. This applies to both healthy volunteers and patients who may be suffering from a particular medical condition.
02
Minors who are capable of providing informed consent may also need study information and consent. In these cases, parental or guardian consent may be required as well.
03
Researchers and study coordinators should provide study information and consent to potential participants in a clear and understandable manner. This ensures that individuals are fully aware of the details of the study and can make an informed decision about their participation.
Remember, the process of filling out study information and consent is important for both the participant and the researchers. It ensures transparency, informed decision-making, and ethical standards are maintained throughout the study.
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Study information and consent refers to the details and permission obtained from participants in a research study.
Researchers or individuals conducting the study are required to file study information and consent.
Study information and consent can be filled out by providing accurate details about the study and obtaining informed consent from participants.
The purpose of study information and consent is to ensure that participants are fully informed about the research study and voluntarily agree to participate.
Study information and consent must include details about the study objectives, procedures, risks, benefits, confidentiality, and participant rights.
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