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Research Consent Form authorization to Disclose Health Information (Parents)Title of research project Determining the Natural and “Unnatural History of Anomalous Aortic Origin of a Coronary Artery
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How to fill out sample combined informed consent

01
Read the entire informed consent form carefully to understand its purpose and provisions.
02
Provide personal information such as name, date of birth, and contact information.
03
Understand the research study or medical procedure for which the consent is being obtained.
04
Familiarize yourself with the risks and benefits involved in participating in the study or procedure.
05
Sign and date the consent form, indicating your agreement to participate or undergo the procedure.
06
If applicable, have a witness sign the form as well.
07
Keep a copy of the signed consent form for your records.

Who needs sample combined informed consent?

01
Researchers and medical professionals conducting studies or performing medical procedures that require informed consent.
02
Individuals participating in research studies or undergoing medical procedures where informed consent is necessary.

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Sample combined informed consent is a document that consolidates various informed consent requirements for research participants into a single form, ensuring that individuals are fully aware of their rights, risks, and the nature of the research.
Researchers or institutions conducting studies that involve human participants are required to file a sample combined informed consent.
To fill out a sample combined informed consent, researchers should provide clear and comprehensive explanations of the study, including its purpose, procedures, risks, benefits, and the rights of participants, along with spaces for participants to sign and date.
The purpose of sample combined informed consent is to ensure that participants are adequately informed about a study and voluntarily agree to participate, thereby protecting their rights and welfare.
The sample combined informed consent must include the study's purpose, procedures, potential risks and benefits, confidentiality assurances, contact information for questions, and participant rights.
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