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** Do not use for collection of biospecimens or research involving genetic/genomic analyses** Informed consent is required to provide potential participants or their legally authorized representatives
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How to fill out informed consent is required

01
Provide a clear and concise explanation of the study to the participant.
02
Discuss the purpose, procedures, risks, and benefits of the study.
03
Allow the participant to ask any questions or seek clarification.
04
Ensure that the participant fully understands the information provided.
05
Obtain written consent from the participant once they are willing and ready to participate.
06
Provide a copy of the informed consent form to the participant for their records.

Who needs informed consent is required?

01
Informed consent is required for any individual who is capable of understanding the study information and making a voluntary decision to participate.
02
This includes adults, adolescents, and minors (with parental or guardian consent).
03
Informed consent is also necessary for vulnerable populations such as prisoners, individuals with cognitive impairments, and those with limited English proficiency.

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Informed consent is when an individual agrees to participate in a study or procedure after being fully informed of all relevant information.
Research institutions, healthcare providers, and researchers are required to obtain informed consent from participants.
Informed consent forms should be written in clear and simple language, presenting all relevant information about the study or procedure.
The purpose of informed consent is to ensure that individuals understand the risks, benefits, and procedures of a study or medical treatment before agreeing to participate.
Informed consent forms should include information about the risks, benefits, alternatives, confidentiality, and contact information for further questions.
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