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STATEMENT OF INFORMED CONSENT FOR PARENTS/GUARDIANS ALL FIELDS MANDATORY: PLEASE PRINT LEGIBLY This parent/guardian consent form is required for ALL youth attending Cadets 2021 National Leadership
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To fill out a statement of informed consent, follow these steps:
02
Read the entire statement carefully to understand the purpose and requirements of the consent.
03
Provide your personal information such as name, age, address, and contact information.
04
Understand the information provided in the statement and make sure you have a clear understanding of the risks, benefits, and alternatives involved.
05
If you have any questions or concerns, consult with the relevant healthcare professional or research coordinator.
06
Sign and date the consent form to indicate your agreement and understanding of the information provided.
07
Keep a copy of the signed statement for your records.
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Note: The specific instructions for filling out a statement of informed consent may vary depending on the context and purpose. Always refer to the provided guidelines or consult with the relevant authority for accurate instructions.

Who needs statement of informed consent?

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A statement of informed consent is typically required in various medical and research settings, including:
02
- Clinical trials
03
- Medical procedures involving potential risks
04
- Research studies involving human subjects
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- Participation in experimental treatments or therapies
06
Any situation where the individual or organization administering the procedure or study requires explicit consent from the participant or patient would necessitate a statement of informed consent.
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The statement of informed consent is a document that outlines the risks, benefits, and alternatives of a medical procedure or research study, and is signed by the participant or patient to indicate their understanding and agreement.
Researchers and healthcare providers are required to file a statement of informed consent with their institutional review board (IRB) or ethics committee before conducting a study or procedure involving human subjects.
The statement of informed consent should be filled out by providing clear and comprehensive information about the study or procedure, including the risks, benefits, and alternatives. Participants or patients should then read and sign the document to indicate their understanding and agreement.
The purpose of the statement of informed consent is to ensure that participants or patients are fully informed about the risks, benefits, and alternatives of a medical procedure or research study, and to protect their rights and well-being.
The statement of informed consent must include information about the nature of the study or procedure, the risks and benefits involved, any potential alternatives, the procedures for data collection and storage, and contact information for the research team.
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