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How to fill out continuing review form
How to fill out continuing review form:
01
Start by carefully reading through the instructions provided with the continuing review form. This will give you a better understanding of what information is required and how to properly fill out the form.
02
Collect all the necessary documents and information that will be needed to complete the form. This may include previous study reports, consent forms, participant tracking listings, adverse event reports, and any other relevant documents.
03
Begin by filling out the basic information section of the continuing review form. This typically includes the study title, principal investigator's name, the study sponsor, and any other identifying information.
04
Provide a brief summary of the study's progress since the last review. Describe any changes made to the study protocol, recruitment strategies, or any adverse events that have occurred during the study period.
05
Fill out the participant information section, which includes details about the number of participants enrolled, any withdrawals or dropouts, and any new participants added since the last review.
06
Review and update the consent process section, ensuring that all participants have provided informed consent and that any changes to the consent form have been documented.
07
Describe any changes made to the study procedures, interventions, or assessments since the last review. This may include changes to the study timeline, recruitment methods, or any modifications to the study protocol.
08
Provide a summary of any adverse events or unanticipated problems that have occurred during the study period. Include details about how these events were addressed and any changes made to the study to prevent similar events in the future.
09
Fill out any additional sections or questions specific to your study or institution as required by the continuing review form.
10
Finally, review the completed form to ensure all information is accurate and complete. Sign and date the form as required and submit it to the appropriate review board or ethics committee.
Who needs continuing review form:
01
Researchers involved in conducting studies that involve human subjects typically need to fill out a continuing review form. This form is a requirement to ensure that the study is still ethically sound and that participant safety and welfare are being adequately protected.
02
Institutional review boards (IRBs) or ethics committees often require researchers to submit a continuing review form at specified intervals to provide updates on the study's progress, any modifications made to the study protocol, and to ensure ongoing compliance with ethical guidelines and regulations.
03
Sponsors of the study or funding agencies may also require researchers to submit a continuing review form as part of their oversight and monitoring processes. This allows them to ensure that the study is progressing as planned and that the research team is adhering to the agreed-upon protocols and regulatory requirements.
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What is continuing review form?
Continuing review form is a document that researchers must submit to the Institutional Review Board (IRB) for ongoing approval of their research protocol.
Who is required to file continuing review form?
Researchers conducting human subjects research are required to file continuing review form.
How to fill out continuing review form?
Continuing review form must be completed with updated information on the research protocol, recruitment methods, and any adverse events.
What is the purpose of continuing review form?
The purpose of continuing review form is to ensure that the research protocol still meets ethical standards and to assess any ongoing risks to participants.
What information must be reported on continuing review form?
Information such as updated research protocol, recruitment methods, adverse events, and any changes to the study team must be reported on continuing review form.
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