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INSTITUTIONAL REVIEW BOARD (IRB)CONTINUING REVIEW APPLICATION Clearly type all portions of this form. 1. STUDY TITLE IRB PROTOCOL NUMBER EXPIRATION DATE OF STUDY APPROVAL* *If IRB approval of your
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How to fill out continuing review application

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How to fill out continuing review application

01
To fill out a continuing review application, follow these steps:
02
Start by reviewing the research protocol and any changes that have been made since the initial review.
03
Gather all the necessary documents and forms required for the application.
04
Complete the application form by providing accurate and detailed information about the study, its objectives, methods, and any potential risks or benefits to the participants.
05
Ensure that all required signatures and approvals are obtained from the appropriate individuals, such as the principal investigator, co-investigators, and institutional review board (IRB) members.
06
Attach any supporting documents, such as consent forms, recruitment materials, and data collection instruments.
07
Carefully review the entire application for any errors or inconsistencies before submitting it.
08
Submit the completed application and supporting documents to the designated IRB office or online platform, following the specified submission guidelines.
09
Monitor the status of the application and respond promptly to any requests for additional information or modifications from the IRB.
10
Once the review process is complete, carefully review and address any concerns or feedback provided by the IRB.
11
If the application is approved, ensure that all approved changes are properly implemented in the ongoing study.
12
If the application is not approved, make the necessary revisions and resubmit the application for further review.

Who needs continuing review application?

01
Continuing review applications are typically required for researchers who are conducting studies that involve human participants.
02
These applications ensure that ongoing research studies meet ethical and regulatory requirements, such as protecting the rights and welfare of the participants.
03
Researchers who have received initial approval for their studies and wish to continue their research beyond the initial approval period usually need to submit continuing review applications.
04
It is important for researchers to consult with their institution's IRB or research ethics committee to determine whether a continuing review application is necessary for their specific study.

What is CONTINUING REVIEW APPLICATION - orra rutgers Form?

The CONTINUING REVIEW APPLICATION - orra rutgers is a fillable form in MS Word extension which can be completed and signed for certain purposes. In that case, it is provided to the exact addressee to provide specific details of certain kinds. The completion and signing is available in hard copy by hand or with a suitable application e. g. PDFfiller. These services help to send in any PDF or Word file without printing them out. It also lets you customize it depending on your needs and put a legal electronic signature. Once done, the user ought to send the CONTINUING REVIEW APPLICATION - orra rutgers to the recipient or several of them by mail or fax. PDFfiller offers a feature and options that make your Word template printable. It provides a variety of options for printing out. It doesn't matter how you'll file a document - in hard copy or by email - it will always look neat and firm. In order not to create a new writable document from scratch all the time, make the original file as a template. Later, you will have a rewritable sample.

CONTINUING REVIEW APPLICATION - orra rutgers template instructions

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Continuing review application is a process through which researchers verify that a study is still meeting ethical and regulatory requirements.
Researchers conducting studies involving human subjects are required to file continuing review applications.
Continuing review applications can be filled out electronically through the institution's research administration system.
The purpose of continuing review application is to ensure the ongoing safety and well-being of research participants.
Continuing review applications must include updated information on study progress, any adverse events, and modifications to the study protocol.
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