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End Clinical Trial Research Screening Adult Consent/Assent Form Version 3.0 Version Date: 17 Jun 2019 SUBJECT IDENTIFICATIONProtocol Title: end (Evaluating Newly Approved Drugs in Combination Regimens
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How to fill out consent and assent form

01
Read and understand the information provided in the consent and assent form.
02
Fill out the participant's personal details, such as name, age, and contact information.
03
Provide any necessary medical history or pre-existing conditions that may affect the study or research.
04
Review the purpose of the study or research and any potential risks or benefits involved.
05
Indicate your consent or assent by signing and dating the form.
06
If applicable, provide the contact information for someone who can be reached in case of emergency.
07
Return the completed form to the designated individual or organization conducting the study or research.

Who needs consent and assent form?

01
Consent and assent forms are required for any study or research involving human participants, especially in fields such as medical, psychological, social sciences, or education.
02
These forms ensure that participants are fully informed of the study's purpose, potential risks, and benefits before they decide to participate.
03
Minors or individuals who are unable to provide informed consent due to cognitive limitations may require an assent form, alongside the consent form from their legal guardians or authorized representatives.
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Consent and assent form is a document that explains the research study and allows individuals to voluntarily agree to participate in the study (consent) or for minors to agree to participate with parental permission (assent).
Researchers conducting a study involving human subjects are required to obtain and file consent and assent forms.
Consent and assent forms can be filled out by providing the required information about the study, risks and benefits, participant rights, and any other relevant details in a clear and understandable manner.
The purpose of consent and assent form is to ensure that participants are informed about the study, voluntarily agree to participate, and understand their rights.
The consent and assent form must include information about the study purpose, procedures, risks and benefits, confidentiality, participant rights, and contact information for questions or concerns.
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