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Office for Human Research ProtectionsGuidance on Reporting Incidents to OHRPKristina Horror, Ph.D. Director, Division of Compliance Oversight July 24, 2014 1Office for Human Research ProtectionsOverview
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How to fill out research protections:

01
Start by familiarizing yourself with the regulations and guidelines relevant to your specific research field. This may include reviewing federal, state, and institutional policies on research protections.
02
Identify the appropriate forms or applications required to fill out research protections. These forms can typically be found on your institution's research website or through the relevant regulatory body.
03
Carefully read through each section of the form, paying close attention to the instructions and any specific requirements outlined. Make sure you fully understand the purpose of each section and what information is expected from you.
04
Gather all necessary documentation and information before starting to fill out the form. This may include your research proposal, informed consent forms, data management plans, conflict of interest disclosures, and any other relevant supporting documents.
05
Begin filling out the form, one section at a time, following the provided format and guidelines. Be accurate and thorough in your responses, providing all requested information and supporting documentation as required.
06
When completing the form, remember to pay attention to any requirements for formatting, signatures, or attachments. Double-check that you have provided all necessary information and have met all stated deadlines.
07
If you come across any uncertainties or questions while filling out the form, consult with a research compliance officer or other relevant personnel who can provide guidance and clarification.
08
Once you have completed the form, review it carefully before submission. Ensure that all information is accurate and consistent, and that all required signatures and attachments are included.
09
Submit the form according to the designated submission process, following any additional instructions provided. Keep copies of your completed form and supporting documents for your records.

Who needs research protections:

01
Researchers conducting studies involving human subjects, animals, or sensitive data.
02
Institutions, universities, or organizations that oversee and facilitate research activities.
03
Funding agencies or sponsors that provide financial support for research projects.
04
Institutional review boards (IRBs) or ethics committees responsible for reviewing and approving research protocols.
05
Participants or subjects involved in research studies, who deserve protection and ethical treatment throughout the research process.
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Research protections refer to the measures put in place to ensure the safety, privacy, and rights of participants involved in research studies.
Researchers and institutions conducting research studies are required to file research protections.
Research protections are typically filled out by following the guidelines and protocols set by the Institutional Review Board (IRB) or ethics committee overseeing the research study.
The purpose of research protections is to uphold ethical standards, ensure participant safety, and maintain the integrity of the research data.
Research protections must include details about the study design, risks and benefits to participants, informed consent process, and confidentiality procedures.
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