See the Glossary for more terms.
This SOP is for grants only.
This standard operating procedure (SOP) includes the following sections: Purpose, Procedure, Contacts, and Links.
To ensure that institutions receiving an HHS grant for activities involving human subjects comply with federal, HHS, and NIAID regulations.
NIH sets policies for human subjects research according to federal law 45 CFR 46, Protection of Human Subjects, which applies to all domestic and international grants.
Find NIH policies in these documents:
Before preparing a grant application, first determine whether your project qualifies as human subjects research.
If you are proposing to conduct an investigator-initiated clinical trial, follow NIAID's mandatory approach. For details, go to Investigator-Initiated Clinical Trial Resources and the Investigator-Initiated Clinical Trial Planning and Implementation Awards SOP.
Make sure you address protection of human subjects (risk, adequacy of protection against risks, potential benefits of the research to subjects, and importance of the knowledge gained), data and safety monitoring, and the inclusion of women, children, and minorities.
Inadequate protection or inclusion plans may negatively affect your overall impact score. See the SF 424 Application Guide for more information.
If there is a scientific rationale for examining subpopulation differences in a foreign population, consider designing your study to accommodate those differences, and discuss inclusion of the groups in your application. For details, see NIH Policy and Guidelines on the Inclusion of Women and Minorities as Subjects in Clinical Research.
Be aware of financial conflicts of interest. See Financial Relationships and Interests in Research Involving Human Subjects and the Financial Conflict of Interest for Awardees SOP. If you identify a conflict, find a way to reduce, eliminate, or manage it, and notify the chief grants management officer that you've taken those steps.
For more help in writing an application, read our NIAID Human Subjects Application and Grant Handbook.
Registering and submitting data. You must register applicable clinical trials—see the glossary term applicable clinical trial—on ClinicalTrials.gov, and NIH urges you to register all of them. Not registering your trial or submitting annual data is a criminal offense that could have repercussions on your award.
To submit data annually or to register, go to the ClinicalTrials.gov Protocol Registration System. If you have questions, contact your program officer.
Progress report. In the human subjects section of your progress report, create a ClinicalTrials.gov heading. Certify you've completed required submissions by following the instructions on NIH's FDAAA and Clinical Trials Supported by NIH Grants.
For additional information, read:
Your institution must obtain a Federalwide Assurance and register its institutional review board (IRB) or independent ethics committee (IEC) with the HHS Office for Human Research Protections. You must get IRB or IEC approval for your application.
You must also document training for investigators and key staff in the protection of human subjects.
Follow these links:
To protect your subjects from forced disclosure of personal information, you may request a Certificate of Confidentiality. For more information, read our Certificates of Confidentiality SOP.
An application will receive a bar to award if the scientific review group is concerned about the protection of human subjects (a code 44 on the summary statement)—see Human Subjects Involvement Codes.
It can also get a bar for unacceptable gender, minority, or children inclusion—for a list of those codes, see Human Subjects Inclusion Codes.
At the end of the fiscal year, an application may get a restriction—code 48—instead.
For details, read Bars to Grant Awards—Human Subjects SOP.
For grant questions, contact Ann Devine.
For review questions, contact Hortencia Hornbeak.
If you have knowledge to share or want more information on this topic, email email@example.com with this link and your message. Thanks for helping us clarify and expand our knowledge base.
Clinical Terms of Award at NIAID's Human Subjects Resources
Human Subjects SOPs
Trans NIAID Clinical Research Toolkit
ClinRegs—for country-specific clinical research regulatory information, including comparison information, presented in plain language.
Data and Safety Monitoring and Further Guidance for Phase I and II
45 CFR 46, Protection of Human Subjects, HHS
Clinical Trial Safety Monitoring and Reporting Requirements Flowchart
Guidance on Informed Consent for In Vitro Diagnostic Device Studies Using Leftover Human Specimens that are Not Individually Identifiable, FDA
Guidance on Research Involving Coded Private Information or Biological Specimens, OHRP
HHS Provides Guidance on Financial Relationships and Interests in Research Involving Human Subjects
Research Involving Human Subjects, NIH
Office of Biotechnology Activities, NIH
NIAID Clinical Terms of Award Restriction for China
NIH's Office of Extramural Research
NIH Grants Policy Statement
Policies & Standards, HHS
Protection of Human Subjects: Assurance Identification/IRB Certification/Declaration of Exemption form
Research Ethics Training Curriculum by Family Health International
Special Protections for Children as Research Subjects, OHRP
Privacy Act of 1974
Last Updated April 22, 2016
Last Reviewed August 18, 2014