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Consent Control Version 4. 11102013.CONTROL PARTICIPANT CONSENT FORM Investigating mutational signatures in cancer and other inherited disorders REC reference number: 13/EE/0302 Chief investigator:
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Start by obtaining the control participant consent form template.
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Read and familiarize yourself with the contents of the form.
03
Ensure that all necessary information is properly filled out, including the name and contact details of the control participant.
04
Clearly outline the purpose of the study or research project in the form.
05
Explain the procedures involved and any potential risks or benefits associated with participation.
06
Provide a clear statement regarding the voluntary nature of participation and the participant's right to withdraw at any time.
07
Include any necessary signatures or witness signatures to validate the consent.
08
Double-check the completed form for accuracy and completeness before finalizing it.

Who needs control participant consent form?

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Researchers or organizations conducting studies or research projects involving control participants need to obtain control participant consent forms.
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Control participant consent form is a document that must be signed by individuals who participate as a control group in a research study.
Researchers conducting a study that involves a control group are required to have participants sign the control participant consent form.
Participants must read the form carefully, sign and date it, and provide any requested personal information.
The purpose of the control participant consent form is to ensure that participants understand and agree to be part of the control group in a research study.
The control participant consent form should include details about the study, the participant's rights, risks and benefits of participation, confidentiality measures, and contact information for questions.
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