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FOR IRB USE ONLY Institutional Review Board Continuing Review Application Date Approval Expires: Date Due to IRB: Protocol Title: Principal Investigator: BHC IRB #: Completion and return of this report
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How to fill out 2008 continuing review application

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How to fill out 2008 continuing review application
01
Start by gathering all necessary information and documents needed for the application, such as the study protocol and any changes made since the last review.
02
Review the application form to ensure you understand all the sections and requirements. Familiarize yourself with any specific instructions or guidelines provided.
03
Begin by accurately providing the requested general information, such as the title of the study, principal investigator's name, contact details, and relevant dates.
04
Complete the section on study personnel, including the names and roles of individuals involved in the study. Ensure all information is up to date and accurately reflected.
05
Next, address any changes or amendments made to the study protocol since the previous review. Provide a clear explanation of each modification and its rationale.
06
Evaluate the current status of participant enrollment and any changes in subject populations or demographics. Specify the number of participants enrolled to date.
07
Document any adverse events or unanticipated problems encountered during the study and describe the actions taken to mitigate or address them.
08
Outline the current consent process and provide a summary of any changes in the informed consent form or procedures.
09
Review and update the study procedures section, ensuring all details are accurate and reflect the current study activities.
10
Include any relevant information regarding the storage, handling, and disposal of study materials or collected data.
11
Provide a detailed summary of any new risks or benefits identified since the last review and present any additional safety measures implemented.
12
Conclude the application by ensuring all sections are complete, signatures are obtained from the necessary individuals, and all supporting documents are attached.
13
Lastly, submit the completed and signed application to the appropriate review board or ethics committee for their review and approval.

Who needs 2008 continuing review application?

01
Researchers conducting studies that were initiated or ongoing in the year 2008 and have undergone previous reviews.
02
Institutions or organizations with research ethics committees or review boards responsible for overseeing and monitoring research activities.
03
Ethical or regulatory bodies requiring periodic updates and assessments of ongoing research studies to ensure participant safety and compliance with ethical standards.
Note: The specific requirements for the 2008 continuing review application may vary depending on the jurisdiction and the guidelines set by the relevant research ethics committee or review board. It is essential to consult the specific instructions and guidelines provided by the responsible authority.
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Continuing review application is a process that allows Institutional Review Boards (IRBs) to evaluate ongoing research studies to ensure compliance with regulations and ethical standards.
Researchers conducting human subjects research must file a continuing review application.
Continuing review application can be filled out by providing updated study information, progress reports, and any changes to the protocol or consent forms.
The purpose of continuing review application is to ensure the protection of human subjects participating in research studies and compliance with regulations.
Continuing review application must include updated study information, progress reports, any amendments to the protocol or consent forms, and any adverse events.
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