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APPROVED AS MODIFIED Mar 01, 2014 WIRE? Atrasentan M11-352 Informed Consent US 17 October 2013 RESEARCH SUBJECT INFORMATION AND CONSENT FORM TITLE: A Randomized, Multi country, Multi center, Double-Blind,
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How to fill out an informed consent form:

01
Read the form thoroughly: Start by carefully reading the entire informed consent form. Understand the purpose of the form, the study or medical procedure being undertaken, and any potential risks and benefits associated with it.
02
Seek clarification: If there are any terms or information that you don't fully understand, ask the healthcare professional or researcher for clarification. It's essential to have a clear understanding of what you're consenting to.
03
Provide accurate information: Fill out the sections of the form that require personal information accurately. This may include your name, contact details, medical history, allergies, and any other relevant information. Providing accurate information is crucial for the validity of the consent form.
04
Ask questions: If you have any questions or concerns about the procedure, feel free to ask. It's important to have a clear understanding of what is expected of you, any potential risks, and the anticipated benefits.
05
Sign and date: Once you have filled out the form and have a clear understanding of its contents, sign and date the consent form. This serves as confirmation that you have willingly given informed consent for the study or medical procedure.

Who needs informed consent form:

Any individual who is participating in a research study or undergoing a medical procedure that involves potential risks or impacts their personal privacy should be asked to provide informed consent. This includes patients in a clinical trial, individuals participating in psychological or sociological studies, and patients undergoing surgical or experimental treatments. Informed consent ensures that individuals have a full understanding of the nature of the study or procedure and are willingly agreeing to participate.

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Informed consent form is a document that provides all the necessary information and details about a research study or medical procedure to the participant or patient. It ensures that the individual understands the risks and benefits involved and voluntarily agrees to participate or undergo the procedure.
Researchers, healthcare providers, and medical professionals are required to file informed consent forms with participants or patients before conducting any research study or medical procedure.
To fill out an informed consent form, one must carefully read and understand all the information provided, ask any questions they may have, and then sign the form to indicate voluntary agreement to participate or undergo the procedure.
The purpose of an informed consent form is to ensure that individuals have full knowledge of the risks, benefits, and procedures involved in a research study or medical procedure, and to make an informed decision about their participation.
An informed consent form must include details about the research study or medical procedure, potential risks and benefits, confidentiality of information, voluntary participation, contact information for questions, and the individual's rights.
The deadline to file informed consent forms in 2023 may vary depending on the specific research study or medical procedure, and should be clearly stated on the form or communicated by the researcher or healthcare provider.
The penalty for late filing of informed consent forms may include delays in conducting the research study or medical procedure, potential legal implications, and negative consequences for the participant or patient's health and well-being.
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