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___ NEBRASKA\'S HEALTH SCIENCE CENTEROFFICE OF REGULATORY AFFAIRS (ORA)Institutional Review Board (IRB)CONTINUING REVIEW OF BIOMEDICAL RESEARCH1. IRB #:2. TITLE OF PROTOCOL:3. PRINCIPAL INVESTIGATOR
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01
To fill out a continuing review of biomedical, follow these steps:
02
Start by reading the instructions provided by your institution or the governing body.
03
Gather all the necessary documents and information, such as the previous review report, any updated protocols, and any relevant supporting data.
04
Review the previous review report and make note of any changes or updates that need to be addressed in the current review.
05
Fill out the required sections of the continuing review form, providing detailed information about the study, any protocol modifications, any adverse events or experiences, and any measures taken to ensure participant safety.
06
Include any supporting documents or data that are required or helpful for the review.
07
Review and revise your responses for accuracy and completeness.
08
Submit the completed continuing review form along with all the necessary documents to the appropriate authority or review board.
09
Keep a copy of the completed form and documents for your records.
10
Be prepared to respond to any additional questions or requests for clarification that may come up during the review process.
11
Follow any additional instructions or recommendations provided by the review board or governing body.

Who needs continuing review of biomedical?

01
Continuing review of biomedical is often required for individuals or organizations involved in biomedical research or clinical trials that involve human subjects.
02
This may include researchers, principal investigators, research institutions, pharmaceutical companies, or any other entity involved in conducting biomedical studies.
03
The specific requirements for continuing review may vary depending on the governing body or regulations in the particular jurisdiction.
04
It is important to consult the relevant guidelines and regulations to determine if and when continuing review is necessary for your specific situation.

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Continuing review of biomedical research is an ongoing assessment of an active research study that is conducted to ensure the continued welfare of the study participants and compliance with regulatory requirements.
Researchers conducting biomedical studies that are subject to Institutional Review Board (IRB) oversight are required to file continuing reviews.
To fill out a continuing review of biomedical, researchers must complete a standardized form provided by the IRB, which typically includes information on the progress of the study, any changes to the protocol, and any adverse events experienced.
The purpose of continuing review is to ensure that the research is being conducted ethically, to assess the risk-benefit ratio, and to monitor participant safety throughout the study.
Information that must be reported includes the current status of the research, updates on enrollment, any significant modifications to the study, adverse events, and overall findings regarding participant safety.
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