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Informed Consent Form Thank you for your time and your consent to participate in the research project entitled, Association of delivery procedure with AGAR scores among neonates born to healthy Pakistani

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How to fill out informed consent form

01

Step 1: Obtain the informed consent form from the appropriate source.

02

Step 2: Read the form carefully and make sure you understand its contents.

03

Step 3: Fill in your personal information, such as your name, date of birth, and contact details.

04

Step 4: Read the information about the study or procedure for which you are giving consent.

05

Step 5: Discuss any questions or concerns with the researcher or healthcare provider before signing the form.

06

Step 6: Sign and date the form to indicate your consent.

07

Step 7: Keep a copy of the signed form for your records.

Who needs informed consent form?

01

Anyone who is participating in a study or medical procedure that requires informed consent needs to fill out an informed consent form. This includes participants in clinical trials, research studies, surgical procedures, and any other situation where consent is required.

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What is informed consent form?

An informed consent form is a document that ensures a participant understands the nature, risks, and benefits of a medical treatment, procedure, or research study before agreeing to participate.

Who is required to file informed consent form?

Researchers, healthcare providers, or organizations conducting studies or medical treatments involving human subjects are required to file an informed consent form.

How to fill out informed consent form?

To fill out an informed consent form, the participant should read the document thoroughly, ask questions for clarification, provide personal information as required, sign the form, and date it.

What is the purpose of informed consent form?

The purpose of the informed consent form is to protect the participant's autonomy and rights, ensuring they make an informed decision about their participation.

What information must be reported on informed consent form?

The form must include details about the study or treatment, potential risks and benefits, alternative options, confidentiality assurances, and the participant's right to withdraw at any time.

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