Since you seem to be proposing a straightforward study involving non-vulnerable participants and non-sensitive data collection, you will be going through Waldens expedited IRB process. You will need to submit the following documents to obtain IRB approval:
1. completed Form C application, which is an ethics self-check in which you will confirm how you meet the universitys ethical standards. Please note, the information described in your Form C application must match the information in your Form A.
application. Please carefully review both Form A and C before you submit your materials to ensure there are no discrepancies, as this will help minimize delays in your ethics review process.
**If you need to update your Form A, please submit a copy of your revised Form A Word document
2.A copy of the questionnaire/survey you plan to use IS ATTACH. If you are using/modifying any previously published data collection instrument, please also submit documentation of approval to use that tool.
3. A draft copy of the consent form you plan to use. Please use the consent form template available online when creating your consent form draft. Your consent form draft must be submitted as a Word document. COPY CONSENT FORM TEMPLATE IS ATTACH AND NEED TO BE COMPLETED.
4. A Letter of Cooperation outlining the sites specific responsibilities for your project, as well as Waldens responsibilities. Please note, while we do provide a template, we do not require that our form be used. If the organization prefers to document their approval using their own form, that would be fine.
TEMPLATE IS ATTACH AND NEED TOM BE COMPLETED.
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