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Signed Informed Consent Form Dear editor: Our study was not involved with any clinical treatment, and a noninformed consent has been applied to the ethics committee of our hospital. Therefore, our
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How to fill out signed informed consent form

01
Read the informed consent form thoroughly before filling it out.
02
Make sure all sections of the form are completed accurately and truthfully.
03
Sign and date the form in the designated areas.
04
If necessary, have a witness sign the form as well.
05
Keep a copy of the signed form for your records.

Who needs signed informed consent form?

01
Anyone participating in a medical or research study that requires informed consent.
02
Patients receiving medical treatment or procedures, especially those that involve risks or experimental therapies.
03
Participants in clinical trials or research studies that involve human subjects.
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A signed informed consent form is a document signed by a patient or research subject, indicating that they understand and agree to participate in a medical procedure or research study.
The healthcare provider or researcher conducting the procedure or study is required to file the signed informed consent form.
The signed informed consent form should be filled out by the healthcare provider or researcher, and then presented to the patient or research subject for their signature.
The purpose of the signed informed consent form is to ensure that the patient or research subject understands the risks and benefits of the procedure or study, and has voluntarily agreed to participate.
The signed informed consent form must include information about the procedure or study, the risks and benefits, alternative options, confidentiality, and the right to withdraw consent.
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