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Get Request & Consent Form
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How to fill out the Request & Consent Form online
This guide provides clear and supportive instructions on how to complete the Request & Consent Form online. By following the steps outlined, users can ensure that their form is filled out accurately and submitted correctly.
Follow the steps to complete the Request & Consent Form online
- Click ‘Get Form’ button to obtain the form and open it in your chosen online editor.
- In Section 1, the approved agency must fill out their name, the applicant's name, and the applicant's role. This section is typically completed by the agency submitting the vetting request.
- Under the applicant’s purpose, check the appropriate box indicating whether the applicant is an employee, contractor, volunteer, or pursuing other purposes. Make sure to select all relevant groups the applicant will interact with.
- Confirm if the request is mandatory under the Vulnerable Children Act. If yes, specify the check reason by selecting from the given options.
- The agency must provide evidence of identity, completing all mandatory identity checks. The agency representative should confirm the identity of the applicant accurately.
- In Section 2, the applicant should complete their personal information including their name, date of birth, gender, and place of birth.
- The applicant must provide their permanent residential address, ensuring that all mandatory fields are filled in completely.
- In Section 3, the applicant gives consent to release information. They should read through the points carefully and provide their authorisation by signing and dating the form.
- Once all sections are completed, review the entire form for accuracy and completeness. Users can then save the changes, download the form, and proceed to print or share it as necessary.
Complete your Request & Consent Form online today for a seamless vetting process.
The informed consent document should succinctly describe the research as it has been presented in the IRB application. Use the second (you) or third person (he/she) to present the study details. Avoid use of the first person (I). Include a statement of agreement at the conclusion of the informed consent document.
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