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How to fill out continuing review of approved

How to fill out continuing review of approved?

1. Start by gathering all the necessary documentation and materials related to the approved project, such as the original research protocol, consent forms, and any amendments or updates that have been made since the last review.
2. Review the existing research protocol and assess whether any changes or modifications have been made to the study procedures, participants, or any other relevant aspects. If there have been any amendments, make sure to accurately document and describe them in the continuing review form.
3. Evaluate the progress of the study and assess whether it is still in compliance with the ethical and regulatory requirements set forth by the institution or governing body. Consider any adverse events or unexpected outcomes that might have occurred since the last review.
4. Determine whether there have been any changes in the research team or key personnel involved in the project. This includes adding or removing investigators, coordinators, or any other individuals who play a significant role in the study.
5. Verify that all research participants have provided informed consent and are still willing to continue their participation in the study. Document any updated consent forms or re-consenting procedures that were implemented during the ongoing research.
6. Collect and analyze any new data or interim findings that have been obtained since the last review. Assess the validity and reliability of the data, and determine whether it supports the continuation of the study or if any modifications need to be made.
7. Fill out the continuing review form accurately and thoroughly, providing detailed explanations and justifications for any changes or updates that have been made. Include all relevant information required by the institution or governing body, ensuring compliance with the specific guidelines and requirements.

Who needs continuing review of approved?

1. Researchers and investigators conducting studies that have been approved by an institutional review board (IRB) or ethics committee are required to undergo continuing review.
2. Institutions and organizations that oversee the ethical conduct of research, such as universities, hospitals, or research centers, typically mandate continuing review to ensure ongoing compliance with ethical and regulatory standards.
3. Funding agencies or sponsors that support research projects may also require researchers to undergo continuing review as part of their funding agreement, ensuring accountability and monitoring the progress of the study.

Overall, continuing review of approved protocols is necessary to ensure the ongoing ethical conduct of research, protect the rights and welfare of research participants, and maintain compliance with relevant regulations and guidelines.

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