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Official title: A phase 2, open label study of the safety, antiretroviral activity and pharmacokinetics of 3BNC117 during a short analytical treatment interruption in HIV infected subjects NCT number:
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How to fill out non-healthy volunteer consent form

01
Read the non-healthy volunteer consent form carefully before filling it out.
02
Fill in your personal information including your name, address, contact details, and identification number.
03
Provide your medical history, including any previous illnesses, surgeries, or chronic conditions you have had.
04
Answer the questions about your current health status, medications you are currently taking, and any allergies or adverse reactions you have experienced.
05
Review and acknowledge any risks or potential side effects of the study or trial you are volunteering for.
06
Sign and date the consent form to indicate your understanding and willingness to participate as a non-healthy volunteer.
07
Ensure that any additional required fields or sections are filled out accurately and completely.
08
Submit the completed consent form to the appropriate study or trial coordinator.

Who needs non-healthy volunteer consent form?

01
Non-healthy volunteer consent forms are typically required for individuals who do not meet the criteria of being in good health for a specific study or clinical trial.
02
These individuals may have pre-existing medical conditions or illnesses that do not necessarily exclude them from participating but require additional caution and consent.
03
The consent form helps to ensure that non-healthy volunteers understand the risks involved and provide their informed consent to participate.
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Non-healthy volunteer consent form is a document that a volunteer must sign to indicate that they understand the risks and potential outcomes of participating in a non-healthy volunteer program.
Non-healthy volunteers who are planning to participate in a research study or a medical trial are required to file a non-healthy volunteer consent form.
To fill out a non-healthy volunteer consent form, volunteers must read the document thoroughly, understand the information provided, and sign the form to indicate their agreement to participate.
The purpose of a non-healthy volunteer consent form is to ensure that volunteers are fully informed of the risks involved in the study or trial, and to obtain their voluntary agreement to participate.
Non-healthy volunteer consent forms must include information about the potential risks, benefits, procedures, and requirements of the study or trial, as well as contact information for the research team.
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