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For adult patients with cancer (or suspected cancer)england100,000 Genomes ProjectC1Hospital logo hereParticipant consent form If you agree to take part in the 100,000 Genomes Project, please initial every
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How to fill out participant consent form

01
Provide all necessary information about the research study to the participant.
02
Clearly explain the purpose of the study, what will be involved, and any potential risks or benefits.
03
Ensure the participant understands their rights and that their participation is voluntary.
04
Have the participant read and sign the consent form, indicating their agreement to participate.
05
Make a copy of the signed consent form for both the participant and the research team.

Who needs participant consent form?

01
Anyone conducting a research study that involves human participants needs to have a participant consent form signed by each individual participating in the study.
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Participant consent form is a document that outlines the agreement between a participant and a researcher, granting permission for the participant to take part in a research study.
Researchers conducting a study involving human participants are required to have participants fill out and sign a participant consent form.
Participants must read the form carefully, ask any questions they may have, and then provide their signature to indicate their agreement to participate.
The purpose of the participant consent form is to ensure that participants are fully informed about the study, understand their rights, and voluntarily agree to participate.
Participant consent forms typically include information about the study purpose, procedures, risks and benefits, confidentiality, contact information for the researcher, and participant rights.
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