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This document is an application form for expedited review of a research protocol involving human subjects in non-medical research at Stanford University. It outlines the study details, participant
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How to fill out APPLICATION FORM FOR EXPEDITED REVIEW

01
Obtain the APPLICATION FORM FOR EXPEDITED REVIEW from the relevant authority or website.
02
Carefully read the instructions provided with the application form.
03
Fill out your personal information accurately, including your name, address, and contact details.
04
Provide detailed information about the reason for requesting expedited review, including any supporting documents.
05
Check the eligibility criteria and ensure you meet them before submission.
06
Review your application for any errors or missing information before finalizing it.
07
Sign and date the application form where required.
08
Submit the completed application along with any required fees to the designated office or online portal.

Who needs APPLICATION FORM FOR EXPEDITED REVIEW?

01
Individuals or organizations requiring a faster review process for their applications due to time-sensitive circumstances.
02
Applicants dealing with urgent matters such as emergencies, deadlines, or critical situations that necessitate expedited processing.
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An application form is a standardized document to collect relevant information from individuals applying for a particular position, service, or opportunity.
Unlike Full Committee Review, expedited review is done by a single experienced reviewer. The reviewer will evaluate the research for the criteria for approval. Reviewers conducting an expedited review may exercise all of the authority of the IRB except that they may not disapprove a study.
The following types of research are commonly processed under expedited review: Studies involving collection of hair or saliva samples. Studies of blood samples from healthy volunteers. Studies involving noninvasive and minimal risk FDA-approved medical devices (e.g., MRI, electrocardiography, ultrasound, etc.)
An expedited review procedure consists of a review of research involving human subjects by the IRB chairperson or by one or more experienced reviewers designated by the chairperson from among members of the IRB in ance with the requirements set forth in 45 CFR 46.110..
In order to qualify for review via expedited procedures, the research must not be greater than minimal risk and fall into at least one of the expedited categories defined by the federal regulations.
The following types of research are commonly processed under expedited review: Studies involving collection of hair or saliva samples. Studies of blood samples from healthy volunteers. Studies involving noninvasive and minimal risk FDA-approved medical devices (e.g., MRI, electrocardiography, ultrasound, etc.)
An expedited review procedure consists of a review of research involving human subjects by the IRB chairperson or by one or more experienced reviewers designated by the chairperson from among members of the IRB in ance with the requirements set forth in 45 CFR 46.110..

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The Application Form for Expedited Review is a document submitted by individuals or organizations to request a faster evaluation of a project or proposal, typically in regulatory or research contexts.
Individuals or organizations seeking expedited review for their applications, particularly in regulatory processes or grant proposals, are required to file this form.
To fill out the Application Form for Expedited Review, applicants should provide all required personal and project information, clearly justify the need for expedited processing, and submit any necessary supporting documents.
The purpose of the Application Form for Expedited Review is to facilitate quicker decision-making and approval for projects that meet specific criteria, such as urgent public health needs or time-sensitive opportunities.
The form must typically report the applicant's details, project description, justification for expedited review, expected timeline, and any relevant supporting documentation.
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