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ANNEX 1 AF/01012/06 Study Assessment FormProtocol Number: Date (DD/MM/YYY): Protocol Title :Protocol version No... Dated........... Informed Consent Form version No.....dated......... Principal Investigators: Professional
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How to fill out interim institutional review board

01
To fill out an interim institutional review board, follow these steps:
02
Review the guidelines and instructions provided by the specific institution or organization regarding the interim institutional review board process.
03
Obtain the necessary forms or documents required for the review board.
04
Provide all the requested information accurately in the designated sections of the forms.
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Include all relevant supporting documents such as research proposals, informed consent forms, and any other required documentation.
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Ensure that all the information provided is complete and up-to-date.
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Double-check the forms and documents for any errors or missing information before submission.
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Submit the completed forms along with the supporting documents to the designated review board committee or department.
09
Wait for the review board to evaluate the submission and provide feedback or approval.
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Address any concerns or feedback provided by the review board and make any necessary revisions to the application.
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Once the interim institutional review board approves the application, proceed with the research or study as planned.
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Keep a copy of the approved interim institutional review board application and any related correspondence for future reference.

Who needs interim institutional review board?

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Various institutions and organizations require an interim institutional review board. These include:
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- Universities and academic research institutions conducting studies involving human subjects.
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- Hospitals and medical facilities performing clinical trials or research involving patient participants.
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- Pharmaceutical companies and drug manufacturers conducting research on new drugs or therapies.
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- Government agencies carrying out studies or research involving human subjects.
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- Non-profit organizations involved in research or studies that require ethical review.
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- Any entity conducting research or studies with human subjects that are subject to ethical considerations.
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It is important to consult the specific guidelines and requirements of the institution or organization in question to determine if an interim institutional review board is necessary.

What is Interim Institutional Review Board (I-IRB) for Postgraduate ... Form?

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An interim institutional review board (IRB) is a temporary committee established to review research proposals involving human subjects to ensure ethical standards are met, particularly when a regular IRB is not available or during urgent situations.
Researchers or institutions that are conducting studies involving human subjects typically are required to file with an interim institutional review board, particularly if their research cannot wait for normal IRB processes.
To fill out an interim institutional review board application, researchers must provide detailed information about the research study, including its purpose, methodology, potential risks, and how subjects' rights will be protected.
The purpose of an interim IRB is to ensure that research involving human subjects is conducted ethically and in compliance with regulatory requirements, safeguarding the rights and welfare of participants during urgent or transitional phases.
Information that must be reported includes study objectives, participant recruitment methods, informed consent procedures, risks and benefits to subjects, and data handling plans.
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