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PET/CT SCAN REQUISITION AND ELIGIBILITY CHECKLIST Principal Investigator: Dr. Francis Board (BC Cancer) Study Title: Evaluation of the safety and sensitivity protocol # H170090968GaDOTATOC PET/CT
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How to fill out participant information and consent

01
Provide a clear and concise explanation of the study purpose and what participation entails.
02
Include any risks or benefits of participating in the study.
03
Ask participants to provide basic demographic information, such as age, gender, and ethnicity.
04
Clearly outline the consent process and ensure participants understand they have the right to withdraw at any time.
05
Have participants sign a consent form indicating their agreement to participate in the study.

Who needs participant information and consent?

01
Researchers conducting studies or experiments that involve human subjects.
02
Institutional review boards (IRBs) that oversee research involving human participants.
03
Legal entities or funding organizations that require documentation of participant consent.
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Participant information and consent refers to the process of collecting personal data and obtaining permission from individuals to use their information for research or other purposes.
Researchers and organizations conducting studies or projects that involve participants are required to file participant information and consent.
Participant information and consent forms typically include sections for personal details, study objectives, risks and benefits, and a signature to confirm consent.
The purpose of participant information and consent is to protect the rights and privacy of individuals participating in research or other activities.
Participant information and consent forms must include details such as name, age, contact information, study procedures, confidentiality measures, and a statement of voluntary participation.
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