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Get the free INFORMATION SHEET AND CONSENT FORM FOR PARTICIPANTS

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Dr Hayley Scott Priority Research Center for Healthy Lungs Level 2 West Wing, MRI Building Lot 1 Kookaburra Circuit, New Lamb ton Heights NSW 2305 T: 02 4042 0113 Fax: 02 4042 0046Participant Information
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Start by gathering all the necessary information that needs to be filled out on the information sheet and consent form.
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Carefully read the instructions and guidelines provided on the information sheet and consent form.
03
Begin by entering your personal details such as your full name, date of birth, address, and contact information.
04
Fill out any required medical information, such as existing conditions, allergies, or medications.
05
Provide your emergency contact information, including the name, relationship, and contact number of someone who can be reached in case of an emergency.
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Read through the consent section and ensure you understand the terms and conditions.
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Sign and date the information sheet and consent form at the designated areas.
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Review the completed form to ensure all the necessary fields have been filled out accurately.
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Make a copy of the information sheet and consent form for your own records, if required.
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Submit the completed form to the relevant recipient or authority as instructed.

Who needs information sheet and consent?

01
Anyone who is required to provide detailed information and consent in a formal manner may need an information sheet and consent form.
02
This could include patients or participants in medical studies, individuals seeking medical treatment, participants in research projects, applicants for certain jobs, clients of professional services, etc.
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An information sheet is a document that provides detailed information about a particular process, study, or procedure, while the consent portion typically refers to a formal agreement where individuals give their permission to participate or to have their information used.
Individuals and organizations conducting research involving human subjects, or those requiring the use of sensitive data, are typically required to file an information sheet and consent.
To fill out an information sheet and consent, you generally need to provide detailed descriptions of the study, risks, benefits, participant rights, and obtain signatures from participants to confirm their understanding and agreement.
The purpose of an information sheet and consent is to ensure that participants are adequately informed about the study or process they are involved in, allowing them to make an informed decision about their participation.
The information that must be reported usually includes the purpose of the study, procedures involved, potential risks and benefits, what is expected from participants, confidentiality measures, and contact information for questions or concerns.
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