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Continuing Review Form Protocol DeviationSubmit an original plus one copy of the form. Please ensure that all questions are answered in full. Only complete applications will be accepted. Protocol
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How to fill out continuing review form

01
To fill out the continuing review form, follow these steps:
02
Start by reading the instructions provided with the form to understand the requirements and information needed.
03
Gather all necessary documents and information that will be required for filling out the form.
04
Begin with the basic identification details such as the name of the researcher, project title, and date of submission.
05
Provide a brief summary of the project, outlining its objectives and significance.
06
Describe the progress made since the last review, highlighting any changes made to the research plan or methodology.
07
Include any adverse events or incidents that have occurred during the research process and how they were addressed.
08
Review and update the consent form and any participant materials if necessary.
09
Provide information on any new risks or ethical concerns that have emerged since the previous review.
10
If applicable, include any updated information on the composition of the research team or collaborating institutions.
11
Sign and date the form, ensuring all required sections have been completed accurately.
12
Submit the completed form to the designated reviewing authority or ethics committee.
13
Remember to carefully review the form before submission to ensure all required information has been provided and the format is correct.

Who needs continuing review form?

01
Various individuals and organizations may need to fill out the continuing review form, including:
02
- Researchers conducting ongoing research projects that involve human subjects.
03
- Institutions or organizations responsible for overseeing research activities and ensuring ethical compliance.
04
- Ethics committees or reviewing authorities tasked with evaluating and approving research protocols.
05
- Funding agencies or sponsors requiring regular updates on the progress and ethical considerations of funded research projects.

What is Continuing Review - Protocol Deviation Form?

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Continuing review form is a document that must be submitted for the renewal of approval for ongoing research involving human subjects.
The Principal Investigator (PI) and their research team are required to file the continuing review form.
The continuing review form must be completed with current study information, any protocol amendments, and updated consent documents.
The purpose of the continuing review form is to ensure that the research involving human subjects is still ethically valid and that participant safety is protected.
The continuing review form requires reporting on any adverse events, protocol deviations, changes to the study protocol, and any new information related to participant safety.
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