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Memorial Sloan Kettering Cancer Center IRB Number: 93102 A(25) Approval date: 16May2018INFORMED CONSENT FOR CLINICAL RE SEARCH Ascertainment of Peripheral Blood or Saliva Samples for Genetic Epidemiology
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How to fill out informed consent for clinical

01
Read the informed consent document thoroughly.
02
Understand the purpose and procedures of the clinical study.
03
Clarify any doubts or questions with the researcher or healthcare professional involved.
04
Provide all necessary personal and medical information accurately.
05
Sign and date the consent form.
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Keep a copy of the signed consent form for your records.

Who needs informed consent for clinical?

01
Anyone participating in a clinical study or trial as a participant, including patients, healthy volunteers, and individuals involved in the research.
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Informed consent for clinical refers to the process by which a patient voluntarily confirms their willingness to participate in a clinical trial or study after being informed of all relevant facts, including risks and benefits.
Researchers and organizations conducting clinical trials are required to obtain and file informed consent from participants.
To fill out informed consent for clinical, a participant should read the consent form carefully, understand the information provided, ask questions if necessary, and sign the form where indicated.
The purpose of informed consent for clinical is to ensure that participants are fully informed about the study, understand their rights, and voluntarily agree to participate without any coercion.
Informed consent must include information on the purpose of the study, procedures involved, potential risks and benefits, alternatives to participation, and confidentiality assurances.
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