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Start by logging into the system or website where the continuing review form is available.
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Locate the specific continuing review form that needs to be filled out.
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Read through all the instructions and guidelines provided in the form or on the website.
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Begin filling out the form by entering your personal information, such as name, contact details, and any identification numbers required.
05
Provide information about the study or research project for which the continuing review is being conducted.
06
Answer all the questions related to the progress of the study since the initial review, including any changes or updates.
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If there have been any adverse events or unexpected outcomes during the study, make sure to document them accurately.
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Submit the completed continuing review form as per the instructions provided.
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Who needs continuing review - form?

01
Researchers and scientists conducting studies or research projects that involve human subjects need to fill out a continuing review form.
02
Institutional review boards (IRBs) or ethics committees require researchers to undergo a continuing review process to ensure the safety and ethical standards of the study are maintained.
03
Individuals or institutions receiving funding from organizations or agencies may also be required to complete continuing review forms as a condition of the funding agreement.
04
Different guidelines and regulations may apply depending on the country or jurisdiction where the study is being conducted, so it is important to consult the relevant authorities or ethics committees for specific requirements.
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The continuing review form is a document that researchers submit to the Institutional Review Board (IRB) to provide an update on the progress of an ongoing research study.
Researchers who are conducting human subjects research and have received approval from the IRB are required to file a continuing review form.
Researchers must provide a summary of the progress of the study, any adverse events that have occurred, any changes to the protocol, and any new information that may impact the risks and benefits of the study.
The purpose of the continuing review form is to ensure that the study is being conducted ethically and in compliance with regulatory requirements, and to provide an opportunity for the IRB to assess the ongoing conduct of the study.
Researchers must report on the progress of the study, any adverse events, any protocol modifications, and any new information that may impact the risks and benefits of the study.
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