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Consent to take part in a research study: THE WOMEN HEALTH INITIATIVE Long Life Study 2 WHO Clinical Coordinating Center The Fred Hutchinson Cancer Center Seattle, Washington Principal Investigator:
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Read the consent form carefully to understand the purposes of the study and what is expected of you.
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Provide your personal information as requested in the form.
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Sign and date the consent form to indicate your willingness to participate.
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Who needs consent to take part?

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Anyone who wishes to participate in the study or research project must provide consent to take part.
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Consent to take part is a document that gives permission for an individual to participate in a specific activity or study.
Anyone who wishes to participate in the activity or study is required to file consent to take part.
Consent to take part can be filled out by providing personal information, agreeing to terms and conditions, and signing the document.
The purpose of consent to take part is to ensure that individuals are aware of the risks and benefits of participating in the activity or study and are giving their voluntary permission to take part.
Consent to take part must include information about the activity or study, potential risks or benefits, confidentiality agreements, and contact information for questions or concerns.
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