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Participant Information and Consent Form Title: Short title: Towards adequate national provision of genomic testing in pregnancy Genomics & Pregnancy the Gap study Protocol number: kWh — R14/7;

How to fill out participant information and consent

1. Start by gathering all the necessary information from the participant. This may include their full name, contact details, age, and any other relevant demographic information. Make sure to explain why these details are needed and how they will be used.
2. Provide a clear and concise consent form for the participant to read and understand. This consent form should outline the purpose of the study or activity, any potential risks involved, and the participant's rights. Use plain language and avoid complex technical terms to ensure easy comprehension.
3. Give the participant enough time to carefully read and consider the consent form. Encourage them to ask any questions they may have before proceeding. It is crucial to respect their autonomy and ensure they fully understand what they are agreeing to.
4. Once the participant feels comfortable and fully informed, ask them to provide their signature or other form of consent. This could be a physical signature on a printed document, an electronic signature, or any other agreed-upon method for indicating consent.
5. Store the participant information and consent forms securely, ensuring that they are protected and kept confidential. Follow any relevant data protection regulations or guidelines to safeguard the privacy of the participants.

Who needs participant information and consent?

1. Researchers conducting scientific studies typically require participant information and consent. This ensures that they have accurate data and ethical approval for their research.
2. Organizations hosting events or workshops that involve the participation of individuals may also need participant information and consent. This helps them manage logistics and communicate with participants effectively.
3. Medical professionals and healthcare providers often require participant information and consent for various procedures or treatments. This is essential for ensuring patient safety and adhering to ethical standards of healthcare.

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What is participant information and consent?

Participant information refers to the details of individuals who are taking part in a study or research. Consent is the permission granted by participants to be involved in the study after being informed about the purpose, risks, and benefits.

Who is required to file participant information and consent?

Researchers, scientists, or individuals conducting a study or research involving participants are required to file participant information and consent.

How to fill out participant information and consent?

Participant information and consent forms are typically filled out by providing personal details of the participant, explaining the purpose of the study, risks involved, benefits, and obtaining the participant's signature as consent.

What is the purpose of participant information and consent?

The purpose of participant information and consent is to ensure that individuals are fully informed about the study they are participating in, their rights as participants, and to obtain their permission to take part.

What information must be reported on participant information and consent?

The participant's personal details, the purpose of the study, risks, benefits, and the participant's consent must be reported on the participant information and consent form.