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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. Read the instructions provided by your institution or ethics committee carefully. They will provide specific guidance on how to complete the continuing review form.
2. Start by entering the necessary information at the top of the form, such as the title of your research project, the dates covered by the review, and your contact information.
3. Provide a brief summary of the progress of your research since the last review. Include any significant findings, changes to the study design, or modifications to the informed consent process.
4. Evaluate the risks and benefits of your research. Describe any adverse events or unexpected outcomes that have occurred and provide an analysis of whether they impact the continuation of the study.
5. Review your study procedures, including recruitment methods, data collection processes, and any revisions made to the protocol. Ensure that they align with ethical principles, regulatory requirements, and any feedback received during previous reviews.
6. Assess the informed consent process. Confirm that participants are still being adequately informed about the study and provide updates on any changes made to the consent form.
7. Consider any ethical, legal, or social implications that have arisen during the course of your research. Discuss any steps you have taken to address these issues and ensure compliance with relevant guidelines.
8. Describe any ongoing monitoring or oversight activities, such as data safety monitoring board reviews or audits, and provide an overview of the findings or recommendations from these activities.
9. Review and update any conflicts of interest disclosures. Ensure that you and your research team have disclosed any potential conflicts of interest, financial or otherwise, that may impact your research.
10. Finally, sign and date the form, and submit it to the appropriate review board or ethics committee for their review and approval.

Who needs continuing review of research?

1. Researchers conducting studies involving human subjects typically need to undergo continuing reviews of their research.
2. Institutions, such as universities, medical centers, or other organizations that oversee research, require continuing reviews to ensure compliance with ethical standards and regulations.
3. Ethics committees or institutional review boards (IRBs) are responsible for conducting continuing reviews to evaluate the ongoing ethical acceptability of the research and to protect the rights and welfare of human participants.

For pdfFiller’s FAQs

What is continuing review of research?

Continuing review of research is the process by which an Institutional Review Board (IRB) evaluates the progress of an ongoing research study to ensure the protection of human subjects.

Who is required to file continuing review of research?

Researchers conducting studies involving human subjects are required to file continuing review of research.

How to fill out continuing review of research?

Continuing review of research can be filled out by submitting the appropriate forms and documentation to the IRB overseeing the study.

What is the purpose of continuing review of research?

The purpose of continuing review of research is to ensure that the study continues to meet ethical standards and regulatory requirements.

What information must be reported on continuing review of research?

Information such as any changes to the study protocol, recruitment methods, consent forms, and any adverse events must be reported on continuing review of research.

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