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This document outlines the procedures and guidelines set by the Chicago Department of Public Health for the Institutional Review Board (IRB) overseeing research involving human subjects. It details
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How to fill out Chicago Department of Public Health Institutional Review Board Procedures
01
Obtain the Chicago Department of Public Health Institutional Review Board Procedures document.
02
Review the purpose and scope of the procedures outlined in the document.
03
Identify the research project that requires IRB review.
04
Complete the IRB application form as detailed in the procedures.
05
Gather all necessary supporting documents, such as consent forms and data collection instruments.
06
Submit the completed application and supporting documents to the IRB for review.
07
Address any feedback or revisions requested by the IRB.
08
Await approval from the IRB before commencing the research project.
Who needs Chicago Department of Public Health Institutional Review Board Procedures?
01
Researchers or organizations conducting studies involving human subjects within Chicago.
02
Educational institutions planning research involving student participation.
03
Public health officials and program evaluators designing interventions requiring ethical oversight.
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What are the requirements for IRB approval?
Specific criteria used by the IRB to determine the approval period (e.g., the nature of the study and risks posed by the study; the degree of uncertainty regarding the risks involved; the vulnerability of the subject population; the experience of the investigator; the IRB's previous experience with the investigator and
What 5 types of people must be present at an Institutional Review Board?
Under the Common Rule, IRBs must have at least five members and include at least one scientist, one non-scientist, and “one member who is not otherwise affiliated with the institution and who is not part of the immediate family of a person who is affiliated with the institution”(§ 46.107(d)).
What is the mandate of the Institutional Review Board IRB?
The IRB is concerned with protecting the welfare, rights, and privacy of human subjects. The IRB has the authority to approve, exempt, disapprove, monitor, and require modifications in all research activities that fall within its jurisdiction as specified by both the federal regulations and institutional policy.
What is the process of the Institutional Review Board?
The IRB office utilizes an initial pre-review screening process, during which an IRB analyst reviews each submission for completeness and compliance. The analyst may ask the PI to make changes to the submission before it is reviewed by the IRB (pre-review).
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What is Chicago Department of Public Health Institutional Review Board Procedures?
The Chicago Department of Public Health Institutional Review Board Procedures outline the process for reviewing research involving human subjects to ensure ethical standards and compliance with regulations.
Who is required to file Chicago Department of Public Health Institutional Review Board Procedures?
Researchers and organizations conducting studies involving human participants within the jurisdiction of the Chicago Department of Public Health are required to file these procedures for approval.
How to fill out Chicago Department of Public Health Institutional Review Board Procedures?
To fill out the Chicago Department of Public Health Institutional Review Board Procedures, researchers must complete the designated application forms, provide a detailed study protocol, and submit required documentation regarding informed consent and data protection.
What is the purpose of Chicago Department of Public Health Institutional Review Board Procedures?
The purpose of these procedures is to protect the rights and welfare of human subjects involved in research and to ensure that all studies comply with ethical and regulatory standards.
What information must be reported on Chicago Department of Public Health Institutional Review Board Procedures?
Researchers must report information such as study objectives, methodology, participant recruitment strategies, informed consent procedures, and plans for data management and confidentiality.
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