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PREAPPROVED: APPROVED: OMB OM BNO. NO.(TBD) 06940135 FORM U.S. DEPARTMENT OF COMMERCE Bureau of Industry and Security Date Received (Leave Blank) U.S. NUCLEAR REGULATORY COMMISSION Office of Nuclear
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How to fill out additional protocol report:

01
Start by gathering all relevant information and documentation required for the report. This may include data, evidence, observations, and any other supporting materials that are necessary.
02
Begin by providing a clear and concise introduction to the report. This should include details such as the purpose of the report, its scope, and any specific guidelines or instructions that need to be followed.
03
Proceed to the main body of the report, where you will outline the specific sections and information that need to be included. This may vary depending on the nature of the report and its intended audience.
04
Ensure that each point is addressed thoroughly, providing accurate and objective information. Use clear and concise language, avoiding any unnecessary jargon or technical terms that may confuse the reader.
05
Consider including any relevant data or statistics in the report, using graphs, charts, or tables to present the information in a visually appealing and easy-to-understand manner.
06
Conclude the report by summarizing the main findings, conclusions, and recommendations, if applicable. This section should provide a concise overview of the report and its key points.
07
Before submitting the report, review it thoroughly for any errors, inconsistencies, or omissions. Proofread the document to ensure proper grammar, spelling, and punctuation, as these details are crucial in maintaining a professional and credible report.
08
Finally, submit the report to the designated recipients or authority, following any specific submission requirements or protocols that may be in place.

Who needs additional protocol report:

01
Organizations conducting research studies or experiments that involve human subjects.
02
Regulatory agencies overseeing and monitoring these research activities.
03
Institutional Review Boards (IRBs) or Ethics Committees responsible for reviewing and approving research protocols.
04
Researchers and principal investigators involved in the study, as they need to document adherence to ethical guidelines and protocols.
05
Funding agencies that require reports to ensure compliance and appropriate use of funds.
06
Other stakeholders involved in the research process, such as sponsors or external collaborators, who may need to review the protocol and its updates.
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Additional protocol report is a document that provides additional information or details beyond what is typically required.
Entities or individuals mandated by law or regulatory bodies are required to file additional protocol reports.
To fill out an additional protocol report, one must provide all required information accurately and completely as specified by the governing body.
The purpose of an additional protocol report is to ensure transparency, compliance, and accountability in specific processes or activities.
The information that must be reported on an additional protocol report may vary depending on the requirements set forth by the governing body.
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