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NATIONAL WOMEN HOSPITAL Phone: Fax: Address: Postal Address:(09) 307 4949 093754344 Level 9 Support Building Auckland City Hospital Private Bag 92024 AucklandPARTICIPANT INFORMATION AND CONSENT FORM You

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How to fill out participant information and consent

01

To fill out participant information and consent, follow these steps:

02

Start by collecting all the necessary information from the participant, such as their full name, date of birth, address, and contact details.

03

Create a consent form that includes all the relevant sections and statements. This form should clearly explain the purpose of the study or project, the participant's rights and obligations, and any potential risks or benefits involved.

04

Provide a clear and concise set of instructions for the participant to fill out the form. Make sure they understand each section and the information required.

05

Have the participant read and understand the entire consent form. Answer any questions or concerns they may have.

06

Ask the participant to sign and date the form, indicating their informed consent and agreement to participate.

07

Collect any additional supporting documents or information that may be required, such as proof of identification or medical history.

08

Safely store the participant's information and consent form, ensuring it remains confidential and secure.

09

Periodically review and update the participant information and consent process to ensure compliance with relevant regulations and ethical standards.

Who needs participant information and consent?

01

Participant information and consent are required by any individual or organization conducting studies, research projects, clinical trials, or any activity involving the participation of individuals.

02

This may include academic researchers, pharmaceutical companies, healthcare providers, government agencies, and any other entities that require personal information and consent from participants.

03

Obtaining participant information and consent is essential to ensure ethical practices, protect participants' rights, and comply with legal and regulatory requirements.

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What is participant information and consent?

Participant information and consent refers to the process of providing individuals with details about a study or research project, as well as obtaining their agreement to participate.

Who is required to file participant information and consent?

Researchers and organizations conducting studies or research projects involving human participants are required to file participant information and consent.

How to fill out participant information and consent?

Participants should be provided with clear, concise information about the study, risks, benefits, and their rights. Consent should be obtained in writing.

What is the purpose of participant information and consent?

The purpose of participant information and consent is to ensure that individuals have the necessary information to make an informed decision about participating in a study or research project.

What information must be reported on participant information and consent?

Participant information and consent forms should include details about the study objective, risks and benefits, confidentiality, voluntary participation, and contact information for questions.

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