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This form is used to request an extension for research protocols approved by the Institutional Review Board (IRB) at San Jose State University for collecting data beyond the original approval expiration
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How to fill out San Jose State University Human Subjects-Institutional Review Board Extension Request

01
Begin by downloading the San Jose State University Human Subjects-Institutional Review Board Extension Request form from the university's official website.
02
Fill in the title of your project at the top of the form.
03
Include your contact information, such as your name, email address, and phone number.
04
Indicate the original IRB approval date and provide the protocol number for your study.
05
Outline the reasons for the extension request, ensuring to explain any changes in the study timeline or scope.
06
Provide a brief summary of what has been completed so far and the anticipated completion date.
07
Ensure that all relevant supporting documents are attached, such as consent forms or additional participant information.
08
Review the form for accuracy and completeness before submission.
09
Submit the form to the IRB office via the indicated submission method.

Who needs San Jose State University Human Subjects-Institutional Review Board Extension Request?

01
Researchers conducting studies involving human subjects at San Jose State University who require additional time to complete their projects.
02
Any faculty or student needing an extension on their approved IRB protocols for ongoing research.
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People Also Ask about

The purpose of IRB review is to assure, both in advance and by periodic review, that appropriate steps are taken to protect the rights and welfare of humans participating as subjects in the research.
IRB Approval An Institutional Review Board (IRB) must approve the protocol you propose to employ in your research involving human subjects. However, this IRB approval is no longer required prior to review of your NIH grant application.
Informed consent involves providing a potential subject with adequate information, facilitating comprehension of that information, providing ample opportunity for questions from the subject, and continuing to provide them information as the clinical investigation progresses.
An institutional review board (IRB) is a committee that has been formally designated to approve, monitor, and review biomedical and behavioral research involving humans. It often conducts some form of risk-benefit analysis in an attempt to determine whether or not research should be done.
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.
The IRB reviews the informed consent process to help to make sure that the study details are communicated in language that is readily understandable to the person who may volunteer to be a research subject. The informed consent process includes: Background information about why the study is being done.
The IRB is charged with the responsibility of reviewing, prior to its initiation, all research (whether funded or not) involving human participants. The IRB is concerned with protecting the welfare, rights, and privacy of human subjects.
The primary role of the Institutional Review Board (IRB) is to protect the rights and welfare of human research participants.
What is the Institutional Review Board? -a committee that has been formally designated to approve, monitor, and review biomedical and behavioral research involving humans with the aim to protect the rights and welfare of the research subjects.

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The San Jose State University Human Subjects-Institutional Review Board Extension Request is a formal application submitted to extend the approval of research involving human subjects beyond the original timeline set by the IRB.
Researchers who have ongoing studies that involve human subjects and require additional time beyond the initial approval period are required to file the San Jose State University Human Subjects-Institutional Review Board Extension Request.
To fill out the Extension Request, researchers must complete the designated form, provide updated information about the study, including changes to protocols, participant recruitment, and any relevant data collected, and submit it to the IRB for review.
The purpose of the Extension Request is to ensure that ongoing research studies continue to meet ethical standards and regulatory requirements for the protection of human subjects after the initial approval period has expired.
The information that must be reported includes the current status of the research, any changes to the research protocol, updates on participant recruitment, data collection, and any adverse events that may have occurred during the study.
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