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SAINT LOUIS UNIVERSITY Central IRB Submission Authorization FormINSTRUCTIONS FOR INVESTIGATORS REQUESTING USE OF A CENTRAL IRB This form should be used by investigators who want to submit to partner
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How to fill out central irb submission authorization

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How to fill out central irb submission authorization

01
Gather all necessary documents required for the central IRB submission authorization.
02
Log in to the central IRB submission system.
03
Select or create a new project for which you need the authorization.
04
Provide all project details and information accurately.
05
Upload all the required supporting documents, such as study protocols, consent forms, recruitment materials, etc.
06
Review the submission for any errors or missing information.
07
Submit the authorization request.
08
Wait for the central IRB to review and approve the submission.
09
If any revisions or additional information is requested, provide it promptly.
10
Once approved, download or print the central IRB submission authorization document for your records.

Who needs central irb submission authorization?

01
Researchers or organizations conducting research involving human participants that require oversight and approval from a central IRB.
02
Institutions or universities that have a central IRB policy in place and require submission authorization for research projects.
03
Funding agencies or sponsors that mandate central IRB review and approval for projects they fund.

What is Central IRB Submission Authorization Form?

The Central IRB Submission Authorization is a fillable form in MS Word extension that should be submitted to the required address in order to provide certain information. It needs to be filled-out and signed, which is possible manually, or with the help of a particular software such as PDFfiller. It lets you fill out any PDF or Word document right in the web, customize it depending on your purposes and put a legally-binding e-signature. Right after completion, you can send the Central IRB Submission Authorization to the appropriate person, or multiple recipients via email or fax. The editable template is printable as well thanks to PDFfiller feature and options presented for printing out adjustment. In both digital and physical appearance, your form should have a organized and professional appearance. You may also turn it into a template to use it later, there's no need to create a new file again. You need just to amend the ready sample.

Central IRB Submission Authorization template instructions

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Central IRB submission authorization is the process of obtaining approval from a centralized Institutional Review Board (IRB) for a research study involving human subjects.
Researchers conducting a research study involving human subjects are required to file central IRB submission authorization.
Central IRB submission authorization can be filled out by submitting the required documents and information to the centralized IRB for review and approval.
The purpose of central IRB submission authorization is to ensure the protection of human subjects participating in research studies by having a centralized IRB review and approve the study protocol.
Central IRB submission authorization requires reporting of study protocol, informed consent forms, recruitment materials, and any potential risks to human subjects.
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