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This form is for research projects that are still in progress and must be completed yearly until project completion.
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How to fill out project continuing review form

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How to fill out Project Continuing Review Form

01
Start by gathering all necessary project documentation.
02
Open the Project Continuing Review Form.
03
Fill in the project title and reference number.
04
Provide a brief summary of the project's objectives and progress so far.
05
List any changes in personnel that have occurred since the last review.
06
Describe any adverse events or issues that have arisen during the project.
07
Indicate if there have been any changes to the project's methodology.
08
Provide updates on participant recruitment and retention.
09
Attach any relevant supporting documentation, such as interim data or reports.
10
Review the completed form for accuracy before submission.

Who needs Project Continuing Review Form?

01
Researchers conducting studies that require ongoing assessments.
02
Institutional Review Boards (IRBs) overseeing research compliance.
03
Funding agencies that require regular project updates.
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People Also Ask about

A progress report is an institutionally required study update that must be submitted to the JHM IRB at a designated interval. The purpose of the progress report is to ensure the study is being conducted in a compliant manner and there are no issues with the conduct of the research that would prevent continued approval.
The Institutional Review Board (IRB) is an administrative body established to protect the rights and welfare of human research subjects recruited to participate in research activities conducted under the auspices of the institution with which it is affiliated.
Purpose of IRBs Institutional Review Boards, or IRBs, review research studies to ensure that they comply with applicable regulations, meet commonly accepted ethical standards, follow institutional policies, and adequately protect research participants.
Continuing review provides the IRB with an opportunity to determine whether there is any new information that should be considered to represent such a significant new finding and therefore be communicated to subjects who have already enrolled in the research (e.g., important new toxicity information or new adverse
Under FDA regulations, an IRB is an appropriately constituted group that has been formally designated to review and monitor biomedical research involving human subjects. In ance with FDA regulations, an IRB has the authority to approve, require modifications in (to secure approval), or disapprove research.
Institutional Review Board (IRB) The primary purpose of the IRB is to protect the rights and welfare of human subjects involved in research activities being conducted under its authority.
Definition. Continuing review of research refers to an official review which is conducted at a designated interval after a project has received initial review and approval by the Institutional Review Board (IRB) or Exempt Review Committee (ERC).

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The Project Continuing Review Form is a document used to assess the ongoing status of a research project, ensuring that it continues to meet ethical standards and regulatory compliance.
Principal investigators and research teams involved in ongoing studies that have received prior ethical approval are required to file the Project Continuing Review Form.
The Project Continuing Review Form should be filled out by summarizing the progress of the project, any changes that have occurred, and reporting any adverse events or issues related to the research since initial approval.
The purpose of the Project Continuing Review Form is to provide oversight on research activities, ensuring that they remain ethical and within the bounds of the original approval, while monitoring participant safety and well-being.
Information that must be reported includes the current status of the project, updates on recruitment and retention, any significant changes in study protocol, safety reports, and any adverse events that have occurred.
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