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Get the free Continuing Review Submission Form - University of Illinois - chicago medicine uic

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Submit To: Rm 318 Medical Center Administration (MCA) 914 S. Wood Street (M/C 700) Chicago, IL 60612 Continuing Review Submission Form Cancer Centers use only If checked, IRB concurrent submission
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How to fill out continuing review submission form:

01
Start by carefully reading the instructions provided with the form. Make sure you understand the purpose and requirements of continuing review.
02
Gather all necessary documentation, such as previous approval letters, progress reports, and any supporting materials that may be required.
03
Fill out the basic information section of the form, including your name, contact information, and institutional affiliation.
04
Provide the protocol title or identification number of the research study that is undergoing continuing review.
05
Indicate the date when the study was initially approved and provide the expiration date of the current approval. This information is usually found in the original approval letter.
06
Describe any modifications or changes that have been made to the study since the initial approval. This may include changes to the research design, study population, or procedures.
07
Explain in detail any adverse events or unanticipated problems that have occurred during the course of the study. Include the actions taken to address these issues and any changes made to ensure participant safety.
08
Provide a progress report on the study, summarizing the activities that have taken place since the last review. Include information on participant enrollment, data collection, analysis, and any preliminary findings.
09
Submit any additional documents required, such as updated consent forms, recruitment materials, or data analysis plans.
10
Review the completed form for accuracy and completeness before submission. Make sure all required sections have been addressed and any necessary signatures are provided.

Who needs continuing review submission form?

Researchers and institutions involved in conducting human subjects research that has been approved by an Institutional Review Board (IRB) are typically required to submit a continuing review submission form. This form allows the IRB to evaluate the ongoing progress of the research study and determine if it continues to meet ethical and regulatory standards. The form helps ensure that participant rights and safety are protected throughout the duration of the study.
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Continuing review submission form is a document that researchers submit to the Institutional Review Board (IRB) to request a review of an ongoing research study.
The researchers conducting an ongoing research study are required to file the continuing review submission form.
Researchers must provide updates on study progress, adverse events, changes to study protocol, and any other relevant information on the continuing review submission form.
The purpose of the continuing review submission form is to ensure that the research study continues to meet ethical standards and regulatory requirements for the protection of human subjects.
Researchers must report any changes to the study protocol, adverse events, study progress, and any other relevant information on the continuing review submission form.
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