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Title: RR 403 Continuing Review Ongoing Department: Sparrow Institutional Review Board 1.0 Policy: No Investigator has a right to conduct research within this institution. Rather, it is a privilege
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Review the form carefully: Start by thoroughly reading through the form to understand its purpose and the information required.
02
Gather necessary information: Collect all the relevant information needed to complete the form accurately. This may include details about the ongoing study, changes made since the last review, participant information, and any adverse events that have occurred.
03
Complete the study details: Fill in the necessary information about the ongoing study, such as the study title, principal investigator's name, and study start and end dates.
04
Provide a summary: Write a concise summary of the study objectives, design, recruitment methods, and anticipated risks and benefits to participants.
05
Update protocol amendments: If there have been any changes to the study protocol since the last review, clearly outline them and the reasons behind these modifications.
06
Detail participant involvement: Describe the process of participant recruitment, informed consent procedures, and any potential risks involved. Also, mention any measures taken to protect participant privacy and confidentiality.
07
Address adverse events: If any adverse events have occurred during the study, describe them in detail and explain how they were managed and reported.
08
Submit supporting documents: Attach any necessary supporting documents, such as updated consent forms, data collection instruments, or participant information sheets.
09
Complete signature section: Ensure that all required signatures are obtained, including those of the principal investigator and other relevant personnel involved in the study.
10
Review and submit: Before submitting the form, review it for any errors or omissions and make any necessary revisions. Once satisfied, submit the completed form to the appropriate IRB or ethics committee for review and approval.

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Researchers conducting ongoing studies: Individuals or teams involved in conducting research studies that require ongoing review and evaluation by an Institutional Review Board (IRB) or ethics committee need the irb-rr403-continuingreview-ongoing218330 - sparrow form.
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Institutions with IRB oversight: Organizations that have established IRBs or ethics committees responsible for reviewing and approving research protocols need this form for continuing review and oversight of ongoing studies.
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irb-rr403-continuingreview-ongoing218330 - sparrow is a form used for ongoing review of research projects involving human subjects.
The principal investigator of the research project is required to file irb-rr403-continuingreview-ongoing218330 - sparrow.
irb-rr403-continuingreview-ongoing218330 - sparrow should be filled out with updated information on the progress of the research, any adverse events, and any changes made to the protocol.
The purpose of irb-rr403-continuingreview-ongoing218330 - sparrow is to ensure that the research project is conducted ethically, adhering to the approved protocol, and protecting the rights and welfare of human subjects.
Information such as progress of the research, any adverse events, changes to the protocol, and any new information relevant to the study must be reported on irb-rr403-continuingreview-ongoing218330 - sparrow.
The deadline to file irb-rr403-continuingreview-ongoing218330 - sparrow in 2023 is December 31st.
The penalty for the late filing of irb-rr403-continuingreview-ongoing218330 - sparrow may result in the suspension of the research project until the review is completed.
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