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NEW YORK INSTITUTE OF TECHNOLOGYInstitutional Review Board for the Protection of Human ParticipantsNorthern Blvd, Old Westbury, NY 11568 5166867488?http://www.nyit.edu/ospar/irb/LONG CONSENT FORMTemplate
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How to fill out human research protections program

01
Step 1: Get familiar with the ethics guidelines and regulations related to human research protections program.
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Step 2: Identify the specific requirements and forms that need to be filled out for your research project.
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Step 3: Gather all necessary information and documentation for your research, such as informed consent forms, research protocols, and participant information sheets.
04
Step 4: Fill out the necessary forms accurately and completely, ensuring that all required fields are properly filled in.
05
Step 5: Review and proofread the filled-out forms for any errors or inconsistencies.
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Step 6: Submit the completed forms to the appropriate human research protections program office or Institutional Review Board (IRB) for review and approval.
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Step 7: Respond to any feedback or clarifications requested by the review board and make necessary revisions to the forms if required.
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Step 8: Upon receiving approval, retain a copy of the approved forms for your records and proceed with your research project following the protocols and guidelines set forth in the human research protections program.

Who needs human research protections program?

01
Researchers and scientists conducting studies involving human participants.
02
Academic institutions and research organizations that oversee or conduct human research studies.
03
Healthcare professionals involved in clinical trials or medical research.
04
Government agencies and regulatory bodies ensuring compliance with ethical guidelines for human research.
05
Pharmaceutical companies and drug developers testing new drugs or therapies on human subjects.

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The Human Research Protections Program (HRPP) is a framework that ensures the ethical and regulatory oversight of research involving human subjects, aimed at protecting their rights, welfare, and well-being.
Researchers and institutions conducting studies involving human participants are required to file with the Human Research Protections Program to ensure compliance with ethical standards and federal regulations.
To fill out the Human Research Protections Program application, researchers must provide detailed information about the study protocol, informed consent processes, risk assessment, and how participant confidentiality will be maintained.
The purpose of the Human Research Protections Program is to safeguard the rights and welfare of participants in research studies while ensuring that the research is scientifically sound and ethically conducted.
Required information includes study objectives, methodology, participant recruitment strategies, informed consent process, potential risks and benefits, and data management plans.
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