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CONTINUING REVIEW OF RESEARCH PROTOCOLS BIOLOGICAL AND CHEMICAL SAFETY ISSUES Principal Investigator Protocol Number Contact Number Date Protocol Title Type all responses. Handwritten responses will

How to fill out continuing review of research

How to fill out continuing review of research?

1. Start by carefully reading the instructions provided by your institution or the relevant regulatory body. Familiarize yourself with the specific requirements for the continuing review of research process.
2. Gather all the necessary documents and information. This may include the research protocol, consent forms, any changes or modifications made since the last review, adverse events or incidents that occurred during the study, and any other relevant data.
3. Review the research protocol and ensure that it aligns with the current ethical and legal standards. Make any necessary updates or revisions to address any concerns or changes that may have arisen since the initial approval.
4. Provide a detailed summary of the progress made since the last review. Include information about participant enrollment, any changes in the study population, data collected, and any significant findings or outcomes.
5. Describe any adverse events or incidents that have occurred during the research. This may include unexpected side effects, participant complaints, or any other issues that have arisen. Provide a detailed analysis of how these events were addressed, and any steps taken to prevent similar incidents in the future.
6. Evaluate the risks and benefits of the study. Discuss whether the risks still outweigh the potential benefits or if any adjustments need to be made to ensure participant safety and welfare.
7. Consider any modifications or changes that have been made to the research since the last review. Ensure that these modifications have been properly documented, approved, and implemented in accordance with the applicable regulations.
8. Update the consent forms, if necessary, to reflect any changes or new information that may have emerged during the study. Confirm that the consent process is still conducted properly and that participants are appropriately informed about the study.
9. Submit the completed continuing review application, along with all the required documents, to the appropriate review board or regulatory body within the specified timeline.

Who needs continuing review of research?

1. Researchers conducting ongoing studies: Any researcher who is conducting a study that goes beyond the initial approval period typically needs to go through the continuing review process. This ensures that the research is still ethically and legally sound, and that participant welfare is continuously monitored and protected.
2. Institutional or independent review boards: These oversight bodies are responsible for evaluating and approving research protocols. They also conduct continuing reviews to ensure that the research is being conducted in compliance with the approved protocol and any applicable regulations.
3. Regulatory bodies: Depending on the location and nature of the research, regulatory bodies such as government agencies or ethics committees may require researchers to undergo continuing review to maintain compliance with their specific regulations and guidelines.

In summary, the continuing review of research involves filling out an application that provides updates on the progress of ongoing studies, any changes or modifications made to the research, and any adverse events or incidents that occurred. Researchers, review boards, and regulatory bodies are typically involved in this process to ensure that the research is conducted ethically and in compliance with regulations.

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What is continuing review of research?

Continuing review of research is the process of evaluating and monitoring the progress of an ongoing research study to ensure compliance with regulations and ethical standards.

Who is required to file continuing review of research?

Principal Investigators or researchers conducting the study are required to file continuing review of research.

How to fill out continuing review of research?

Continuing review of research forms can typically be filled out online or through the institution's research compliance office.

What is the purpose of continuing review of research?

The purpose of continuing review of research is to ensure the safety of participants, verify compliance with regulations, and assess the progress of the study.

What information must be reported on continuing review of research?

Information such as participant enrollment numbers, adverse events, any protocol deviations, and overall study progress must be reported on continuing review of research.