Get the free Request for Continuing IRB Approval - Catholic Health

CHS IRB Form 100F Title of Study: Legal Services Department Institutional Review Board Phone: (716) 8214477 Fax: (716) 8214465Request for Continuing IRB Approval 1. Title of Protocol2. Contact Information 2.1

How to fill out request for continuing irb

How to fill out request for continuing irb

1. Start by reviewing the guidelines and instructions provided by the institutional review board (IRB) for submitting a request for continuing IRB.
2. Gather all the necessary information and documents required for the request, such as the study protocol, consent forms, participant recruitment materials, and any relevant amendments or updates.
3. Fill out the request form, providing accurate and complete information as requested. This may include details about the study objectives, methods, participant population, recruitment strategies, any potential risks or benefits, and any changes or updates since the last approval.
4. Ensure that all necessary signatures are obtained, including those of the principal investigator, co-investigators, and any other relevant parties involved in the study.
5. Submit the completed request form and accompanying documents to the designated IRB office or online submission system, following the specified submission guidelines and deadlines.
6. Monitor the status of the request and respond promptly to any additional questions or requests for clarification from the IRB.
7. Await the decision of the IRB regarding the request for continuing IRB. This decision may result in approval, approval with conditions, or denial.
8. If approved, ensure that any necessary updates or amendments are promptly submitted to the IRB in accordance with their requirements.
9. If approved with conditions, address and fulfill any specific requirements or recommendations outlined by the IRB before continuing the study.
10. If denied, carefully review the reasons for denial provided by the IRB and consider any necessary revisions or modifications to the study before resubmitting the request.

Who needs request for continuing irb?

1. Researchers or individuals conducting research studies that require approval from an institutional review board (IRB) need to submit a request for continuing IRB. This is typically required for studies that involve human participants and have received initial approval from the IRB. The request for continuing IRB is an ongoing requirement throughout the duration of the study to ensure that any changes or updates are properly reviewed and approved by the IRB.

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What is request for continuing irb?

Request for continuing IRB is a submission made to the Institutional Review Board (IRB) to request approval to extend the duration of an ongoing research study.

Who is required to file request for continuing irb?

The principal investigator or researcher responsible for the study is required to file the request for continuing IRB.

How to fill out request for continuing irb?

The request for continuing IRB must be filled out completely and accurately, including details about the progress of the study, any adverse events, and any changes to the study protocol.

What is the purpose of request for continuing irb?

The purpose of the request for continuing IRB is to ensure that the study is being conducted in compliance with ethical guidelines and regulations, and to protect the rights and welfare of research participants.

What information must be reported on request for continuing irb?

Information such as study progress, adverse events, protocol deviations, and any amendments to the study protocol must be reported on the request for continuing IRB.

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