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Community Healthcare System Central IRB Facilitated Protocol Submission Form Review for Local Context (Form Date: 4/2017) Reason for Submission: Date Submitted: New Protocol: IND/IDE number for investigational drug/device:IRB
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Go to the online portal for facilitated protocol submission form.
02
Create an account or log in if you already have one.
03
Choose the type of protocol you are submitting.
04
Provide all the required information, such as title, investigators involved, and study objectives.
05
Fill out the necessary sections of the submission form, including study design, methods, and anticipated results.
06
Upload any supporting documents, such as research proposals or ethical clearance certificates.
07
Review the form to ensure all information is accurate and complete.
08
Submit the facilitated protocol submission form.
09
Wait for confirmation of submission and any further instructions or feedback from the relevant authority.

Who needs facilitated protocol submission form?

01
Researchers or organizations conducting studies or research projects that require approval or review from the relevant authority.
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The facilitated protocol submission form is a document used to request special permission or guidance in the submission process for protocols.
Researchers or individuals conducting studies that require special accommodation or assistance from the regulatory body may be required to file a facilitated protocol submission form.
To fill out the facilitated protocol submission form, one must provide detailed information about the study, rationale for special accommodation, and any relevant supporting documents.
The purpose of the facilitated protocol submission form is to ensure that studies requiring special accommodations are properly reviewed and approved.
The facilitated protocol submission form typically requires information about the study design, objectives, methods, and any potential risks or benefits.
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