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INFORMED CONSENT AND REQUEST FOR STERILIZATION DO NOT SIGN THIS FORM UNTIL YOU HAVE READ IT AND FULLY UNDERSTAND ITS CONTENTS PATIENT IS NAME The following has been explained to me in general terms
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How to fill out informed consent and request:

01
Begin by carefully reading the informed consent and request form. Make sure you understand all the information provided and ask any questions you may have.
02
Fill in your personal information accurately, such as your full name, date of birth, and contact details. It is important to provide correct information for identification purposes.
03
Pay attention to any checkboxes or options on the form. If there are specific choices or permissions that need to be indicated, mark them accordingly.
04
Provide any additional information or details requested on the form. This may include medical history, current medications, or any relevant information that the requester needs to know.
05
Sign and date the form at the designated spaces. By signing, you are confirming that you have read and understood the information provided and are willingly giving your consent or making the requested request.
06
If necessary, have a witness sign the form as well. Some forms may require a witness signature to ensure the validity and authenticity of the document.
07
Keep a copy of the form for your records before submitting it. It is always a good practice to have a copy of any important documents you sign.

Who needs informed consent and request?

01
Individuals participating in medical research studies or clinical trials may be required to provide informed consent. This ensures that they understand the purpose, risks, and benefits of the study and voluntarily agree to participate.
02
Patients undergoing medical treatments, surgeries, or procedures may be required to provide informed consent. This ensures that they are fully aware of the risks, potential outcomes, and alternative options before proceeding with the treatment or procedure.
03
In certain legal situations, individuals may need to provide informed consent or make specific requests. This can include situations where medical decisions need to be made on behalf of a minor or an incapacitated adult, or when individuals request access to their personal information.
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Informed consent and request is a form that allows individuals to voluntarily agree to participate in a research study or medical procedure after being fully informed about the benefits, risks, and alternatives.
Researchers, doctors, or medical professionals conducting the study or procedure are required to obtain informed consent and request from the participants.
To fill out informed consent and request, the participant must read and understand the information provided, ask any questions they may have, and then sign the form to indicate their voluntary agreement.
The purpose of informed consent and request is to ensure that participants are fully informed about the study or procedure, its potential risks and benefits, and their rights as participants.
Informed consent and request must include details about the study or procedure, potential risks and benefits, the participant's rights, and how their information will be used and kept confidential.
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