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Get the free IRB Expedited Certification Request - kysu

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This document outlines the procedures for requesting expedited certification for research involving human subjects at Kentucky State University, including guidelines for minimal risk research and
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How to fill out irb expedited certification request

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How to fill out IRB Expedited Certification Request

01
Begin by downloading the IRB Expedited Certification Request form from your institution's website.
02
Fill in your project title at the top of the form.
03
Provide your contact information, including your name, email, and phone number.
04
Describe your research project in detail, including objectives and methodologies.
05
Specify the population involved in your study and how you will recruit participants.
06
Indicate the risks involved to participants and how you intend to minimize them.
07
Include a plan for data confidentiality and participant anonymity.
08
Answer questions regarding informed consent and any necessary documentation.
09
Review the form for completeness and accuracy before submission.
10
Submit the completed form to your institution's IRB office for review.

Who needs IRB Expedited Certification Request?

01
Researchers conducting studies that involve minimal risk to participants.
02
Faculty and students involved in academic research projects.
03
Any individual seeking approval for expedited review of their research involving human subjects.
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Greater than minimal risk studies require full committee review, while minimal risk studies may be eligible for expedited review or exempt certification. Call the IRB Analyst of the Day at 415-476-1814 if you are unsure about which level of review is needed.
The Institutional Review Board (IRB) is an administrative body established to protect the rights and welfare of human research subjects recruited to participate in research activities conducted under the auspices of the institution with which it is affiliated.
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.
Expedited 4. Collection of data through noninvasive procedures routinely employed in clinical practice. Non-invasive procedures include, but are not limited to: (1) vaginal swabs that do not go beyond the cervical os; (2) swabs that do not go beyond the rectum; and (3) nasal swabs that do not go beyond the nares
Expedited Research These categories involve collection of samples and data in a manner that is not anonymous and involves no more than minimal risk to subjects. Some examples of expedited research are: studies involving collection of hair, saliva or dental plaque samples. studies of blood samples from healthy
Examples of Commonly Exempted Research The following types of research are commonly processed under exempt review: Research on educational practices or educational curriculums. Benign behavioral interventions with adult subjects. Anonymous surveys or interviews on non-sensitive topics.
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.

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The IRB Expedited Certification Request is a submission to an Institutional Review Board (IRB) that allows researchers to seek expedited review for certain types of research involving minimal risk to participants.
Researchers conducting studies that qualify for expedited review, particularly those involving minimal risk to human subjects, are required to file an IRB Expedited Certification Request.
To fill out the IRB Expedited Certification Request, researchers need to provide detailed information about the study, including the research protocol, informed consent process, and how the study meets the expedited review criteria.
The purpose of the IRB Expedited Certification Request is to facilitate faster review and approval of research proposals that pose minimal risk, thereby speeding up the research process while ensuring ethical standards are met.
The information that must be reported on the IRB Expedited Certification Request includes the study title, principal investigator details, research objectives, study design, participant criteria, informed consent procedures, and potential risks and benefits.
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