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        • 5-Year / 8-Year Duration Rule
        • Addendum to On-Site Research Collaborators (RC) Policies: On-Site RC Conducting Human Subjects Research at NIH
        • Clarification on Searches for Scientific Director and Clinical Director
        • Departing Staff Request to Remove Copies of NIH Records
        • Fair Review Principles for Nominations of Staff Scientists for Associate Scientist and Senior Associate Scientist Titles
        • Guide for Avoiding Undue Foreign Interference with IRP Research
        • Guidelines for Parental/Family Excused Absence for IRTAs, CRTAs, and Visiting Fellows
        • Mandated Training for Scientific Staff Working in NIH Facilities
        • Non-FTE Trainees Exceptional Extension Policy
        • Policy for a Letter of Agreement for Staff Scientists
        • Policy for Non-Renewal of Non-FTE Trainees
        • Policy for Use of Contract Workers to Support Scientific Functions in the IRP
        • Policy on IRP Unpaid Designations and Non-FTE Fellows with Supplemental Funding
        • Policy on Use of English for Official Scientific Communication in NIH Laboratories and Branches
        • Roles of Lab and Branch Chiefs (or Equivalent)
        • Telework Policies for IRTA/CRTA and Visiting Fellows
        • Working with Displaced Title 42 Staff Scientists/Clinicians
      • Quality-of-Life Features
      • Sabbaticals
        • NIAAA Sabbatical Program
        • NEI Sabbatical Program
        • NICHD Sabbatical Program
        • PHS Foreign Work / Study Program Policy
      • Opportunities for Short Assignments / Details at the NIH
    • Tenure in the NIH Intramural Research Program
      • Tenure-Track Overview
      • Search & Selection
        • Search Process for Senior Investigators, Tenure-Track Investigators, Senior Clinicians and Senior Scientists
      • Additional Tenure-Track Policies
      • Resources
      • Policy on IC Tenure Review Committees
      • Tenure Overview
      • Search & Selection
      • Criteria for Tenure at the NIH
      • De-Tenuring Process
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      • The Director’s Challenge Innovation Award Program
        • 2020 Director’s Challenge Awards
        • 2022 Director’s Challenge Awards
        • 2024 Director’s Challenge Awards
      • Early Career (Bridge) Awards Open to IRP Scientists
      • Eligibility of Intramural Investigators for NIH Common Fund Awards
      • K99/R00 Grant Award Information
        • Application Approval Process and Additional Information
        • K99/R00 Environment and Institutional Commitment Statement
        • Update from Scientific Directors
      • NIAID Support of Intramural Biodefense Research from ICs Other Than NIAID
    • Ethical Conduct
      • Research Misconduct
        • Reporting of Research Misconduct Concerns for the NIH Intramural Research Program
        • Taraswi Banerjee, Ph.D.
        • Alfredo R Sancho, Ph.D., M.P.H.
      • Guidelines on Conduct of Research
      • Research Ethics
        • NIH Policies
          • Intramural / Extramural Collaborations
            • NIH Staff Involvement on Extramural Awards - Cooperative Agreements
              • Opportunities for Collaborative Research at the Clinical Center (U01)
              • NIH Bench-to-Bedside Program
            • Activities with Outside Organizations
          • NIH Human Biospecimen Program
            • Frequently Asked Questions
            • List of Biospecimen Liaisons
          • Investigation of Allegations of Research Misconduct
        • NIH Guidelines
      • Authorship Guidelines and Resources
        • Authorship Resources
        • NIH IRP Authorship Conflict Resolution Policy
      • Special Research Considerations
        • Dual-Use Research
        • Policy on the Ordering or Provision of Synthetic Nucleic Acids in the IRP
        • Human Stem Cell Use
          • Human Embryonic Stem Cell (hESCs) Use
          • Induced Pluripotent Stem Cells (iPSCs) Use
          • Human Embryo Research and Cloning Prohibitions
        • Policies & Procedures for Human Fetal Tissue for Non-Transplantation Research Purposes
      • Responsible Conduct of Research Training
        • Instruction in Responsible Conduct of Research - Postdoc IRTA, CRTA, VF, Research Associates
          • Reproducibility Training
          • Introduction to “My Laboratory”
        • Instruction in Responsible Conduct of Research - Postbacs and GPP Students
        • Resources for Training Directors
        • Annual Review of Ethics (Case Studies)
          • Research Cases for Use by the NIH Community
            • 2021 Ethics Case Facilitator Training
      • Government Ethics
        • Guidelines for Non-FTEs (Trainees) for NIH-Related Activities, Outside Activities, and Awards
      • Bioethics
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      • Guide to Training and Mentoring
      • Guidelines for Mentors at NIH
      • Guidelines for Trainees at NIH
      • Guidelines for Annual Progress Review of Trainees
      • Scientific Director Policy Updates for Mentors and Trainees
      • Goals for Enhanced Mentoring in the IRP
      • Mentoring Cases for Discussions
    • Submitting Research Publications
      • Intramural Academic Freedom Guidance
      • Publication and Abstract Review
      • FAQs on Intramural Publication Reviews
      • NIH Publishing Agreement Forms
        • Procedures for Non-Peer-Reviewed Publications
      • PubMed Central (PMC) Deposition Requirements
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FAQs on Intramural Publication Reviews

Table of Contents

  • Manuscript Review
  • When an NIH Disclaimer Statement is Needed
  • Submission to PubMed Central
  • Publishing Options to Comply With the NIH Public Access Policy

Manuscript Review

  1. Can my SD (or delegate) disapprove of my manuscript submission if they disagree with my scientific conclusions?
    No.
  2. Can my SD (or delegate) disapprove of my manuscript submission if I did not get the appropriate human subjects, animal care and use, or biosafety clearances before conducting the work?
    Yes.
  3. If the SD uses iThenticate or Imagetwin platforms to review the manuscript, and calculates a relatively high similarity score, must I edit the manuscript even if I stand by the submission as written?
    No, these tools are meant to be helpful, not proscriptive. Authors should be aware that many journals will use similar software, though, and it would be wise to edit the manuscript to make it clear why there might be a high score.
  4. Do I still need manuscript review if the senior or corresponding author is from another IC, and has submitted the manuscript for review with that IC?
    There is no IRP-wide requirement for review by multiple ICs, but many ICs do require review under these circumstances. It is best to check with your IC for the IC-specific policy.
  5. Do I need manuscript review if I am a middle author and all other co-authors are from extramural universities and institutes?
    Yes.
  6. Do I need manuscript review if I am just submitting to a pre-publication server like bioRxiv?
    Yes.
  7. Do I need manuscript review if I am writing a review article with no new primary data?
    Yes.
  8. Do I need manuscript review if I am a member of an outside consortium, and the consortium is listed as an author?
    Yes. If a reader will be able to identify an individual in a consortium as an NIH IRP researcher, and the work represents official duty activity, the manuscript should be reviewed by the IC and a disclaimer should be provided for any IRP authors. If IRP researchers are listed as part of a consortium that is issuing a policy statement, the IRP researcher should consult with NIH Office of Science Policy in addition to seeking IC review/clearance, as per the Intramural Academic Freedom Guidance.
  9. Do I need manuscript review if I am re-submitting a manuscript to a journal after making revisions?
    Generally, no. However, if the revision represents a substantially different version, leading to substantially different conclusions and/or interpretations, researchers should consider an internal re-review.

When an NIH Disclaimer Statement is Needed

  1. Does the NIH disclaimer need to be included in all manuscripts, no matter the NIH author’s position in the author list?
    Yes, it must be included, e.g. as a statement in the acknowledgments. Some ICs internal manuscript review system provides precise disclaimer language for inclusion.
  2. Does the NIH disclaimer need to be included in review articles or pre-publication articles?
    Yes.
  3. Is there a specific section in a manuscript where the disclaimer must be inserted?
    No. Many authors use the acknowledgement section.
  4. Am I permitted to modify the disclaimer to add additional information?
    Yes.

Submission to PubMed Central (PMC)

  1. Is it correct that, regardless of where the NIH author appears in the author list, the manuscript must be made available in PMC?
    Regardless of where the NIH funded author(s) appears in the author list, the NIH author(s) must comply with the NIH Public Access Policy. Specifically, peer-reviewed manuscripts should be submitted to PubMed Central at the time of acceptance, to be made available in PMC at the time of publication, without embargo. Note that some journals will deposit the material to PMC on behalf of the author, and the author then has no further PMC responsibilities.
  2. Must I submit an accepted paper to PMC if I am a middle author?
    Yes.
  3. Must I submit an accepted paper to PMC if I did not provide final approval to the manuscript and am unable to obtain the final version from the corresponding author?
    You may contact OIR under these circumstances to discuss some possible solutions, at IRPinfo@mail.nih.gov.
  4. What should I do if I submitted a paper to PMC but the status is listed as “stalled”?
    Contact the NIHMS Help Desk at nihms-help@ncbi.nlm.nih.gov.


Publishing Options to Comply With the NIH Public Access Policy

  1. Am I required to purchase an Open Access Package to comply with the NIH public access requirements?
    Authors must select a payment option that allows them to comply with the NIH Public Access Policy, i.e. submitting the accepted peer-reviewed manuscript to PubMed Central (PMC) upon acceptance, with the article to be made available in PMC at the time it is published, without embargo. Some journals offer the option of a cheaper subscription model and a higher-priced open access model. If both models are available and compliant with the policy, the author can choose. However, a subscription model that requires a PMC embargo period is not compliant with the policy. If the open access model is the only compliant option, the author can either select that method or submit to a different journal.
  2. Will purchasing an Open Access Package satisfy my responsibilities to submit to PMC?
    Manuscripts must be submitted to PMC. If the journal will submit the article to PMC (to be made available at the time of publication) as part of its Open Access package, then the author is compliant with the Public Access Policy. If the journal does not submit to PMC, for example it only posts the article free of charge to readers through its own website, then the author must submit to PMC.
  3. My manuscript was accepted but my only option appears to be to purchase an expensive open access package. What should I do?
    If you still want to publish there, you will need to purchase the open access. However, many institutions have open-access agreements with publishers. If one of your coauthors is a member of one of these institutions, the open access fees may be covered by this agreement if the coauthor is listed as the corresponding author. It is important, therefore, to assess a journal’s pricing and publishing policies and before submission.
  4. I have heard there is a limit on how much I am permitted to pay for publication fees – is that true?
    Not as of the date these FAQs were posted., Although such policies are under discussion, they have not yet been finalized or implemented.

This page was last updated on Thursday, May 21, 2026

Main navigation

  • Board of Scientific and Clinical Directors
    • Board of Scientific and Clinical Directors Membership
    • NIH IRP Scientific Directors
    • NIH IRP Clinical Directors
    • Board of Scientific and Clinical Directors Subcommittees
  • Committees Advisory to the DDIR
    • Assembly of Scientists (AOS)
    • Committee on Scientific Conduct and Ethics (CSCE)
    • Central Tenure Committee (CTC)
    • Chairs of the Boards of Scientific Counselors
    • Tenure-Track Investigators Committee
    • Women Scientist Advisors (WSA) Committee
    • Animal Research Advisory Committee (ARAC)
    • Dual Use Research of Concern (DURC) Committee
    • Facilities Working Group
    • NIH Space Recommendation Board
    • PHS Technology Transfer Policy Board
  • Processes for Reviewing NIH Intramural Science
    • Boards of Scientific Counselors (BSC)
      • Process for Appeal to a BSC Review
    • Role and Review of Scientific Directors and Clinical Directors
    • Blue Ribbon Panel Reviews of IC Intramural Research Programs
  • Intramural Program Oversight
    • Electronic Lab Notebooks
      • Intramural Electronic Lab Notebook Policy
      • Frequently Asked Questions About the Use of ELNs at NIH
    • Human Subjects Research
    • Intramural Data Sharing
      • 2023 NIH Data Management and Sharing Policy
      • Genomic Data Sharing
      • Guide to FDAAA Reporting Research Results
        • Assistance Available to Help with Results Reporting to ClinicalTrials.gov
          • Points of Contact for FDAAA Compliance at ICs
    • IRP Research Security
    • Laboratory Safety
    • Management Controls Survey
  • Intramural Administrative Management Council
    • List of Council Members
    • List of Trans-NIH Committees
  • Personnel
    • IPDs and Appointment Mechanisms
      • Official List of Approved Intramural Professional Designations (IPDs)
      • Senior Investigator
      • Investigator
      • Senior Clinician
      • Senior Scientist
      • Assistant Clinical Investigator
      • Staff Clinician
      • Staff Scientist
        • Explanation of Staff Scientist Position and Titles to Academic Colleagues
      • Senior Research Assistant / Research Assistant
      • Adjunct Investigator
      • Scientist Emeritus
      • Intramural Research Training Award (IRTA) Fellow
      • Visiting Fellow
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        • Independent Research Scholar Program
      • Student Opportunities
      • Contractors
      • Guest Researchers / Special Volunteers
      • Research Collaborators
    • Faculty Development
      • OITE/OIR Professional Development Curriculum for NIH Faculty
      • Senior Advisors for Faculty Development
      • Staff Clinician Pathways
    • Policies and Recruitment Processes
      • 5-Year / 8-Year Duration Rule
      • Addendum to On-Site Research Collaborators (RC) Policies: On-Site RC Conducting Human Subjects Research at NIH
      • Clarification on Searches for Scientific Director and Clinical Director
      • Departing Staff Request to Remove Copies of NIH Records
      • Fair Review Principles for Nominations of Staff Scientists for Associate Scientist and Senior Associate Scientist Titles
      • Guide for Avoiding Undue Foreign Interference with IRP Research
      • Guidelines for Parental/Family Excused Absence for IRTAs, CRTAs, and Visiting Fellows
      • Mandated Training for Scientific Staff Working in NIH Facilities
      • Non-FTE Trainees Exceptional Extension Policy
      • Policy for a Letter of Agreement for Staff Scientists
      • Policy for Non-Renewal of Non-FTE Trainees
      • Policy for Use of Contract Workers to Support Scientific Functions in the IRP
      • Policy on IRP Unpaid Designations and Non-FTE Fellows with Supplemental Funding
      • Policy on Use of English for Official Scientific Communication in NIH Laboratories and Branches
      • Roles of Lab and Branch Chiefs (or Equivalent)
      • Telework Policies for IRTA/CRTA and Visiting Fellows
      • Working with Displaced Title 42 Staff Scientists/Clinicians
    • Quality-of-Life Features
    • Sabbaticals
      • NIAAA Sabbatical Program
      • NEI Sabbatical Program
      • NICHD Sabbatical Program
      • PHS Foreign Work / Study Program Policy
    • Opportunities for Short Assignments / Details at the NIH
  • Tenure in the NIH Intramural Research Program
    • Tenure-Track Overview
    • Search & Selection
      • Search Process for Senior Investigators, Tenure-Track Investigators, Senior Clinicians and Senior Scientists
    • Additional Tenure-Track Policies
    • Resources
    • Policy on IC Tenure Review Committees
    • Tenure Overview
    • Search & Selection
    • Criteria for Tenure at the NIH
    • De-Tenuring Process
  • Awards, Fellowships, & Grant Opportunities
    • The Director’s Challenge Innovation Award Program
      • 2020 Director’s Challenge Awards
      • 2022 Director’s Challenge Awards
      • 2024 Director’s Challenge Awards
    • Early Career (Bridge) Awards Open to IRP Scientists
    • Eligibility of Intramural Investigators for NIH Common Fund Awards
    • K99/R00 Grant Award Information
      • Application Approval Process and Additional Information
      • K99/R00 Environment and Institutional Commitment Statement
      • Update from Scientific Directors
    • NIAID Support of Intramural Biodefense Research from ICs Other Than NIAID
  • Ethical Conduct
    • Research Misconduct
      • Reporting of Research Misconduct Concerns for the NIH Intramural Research Program
      • Taraswi Banerjee, Ph.D.
      • Alfredo R Sancho, Ph.D., M.P.H.
    • Guidelines on Conduct of Research
    • Research Ethics
      • NIH Policies
        • Intramural / Extramural Collaborations
          • NIH Staff Involvement on Extramural Awards - Cooperative Agreements
            • Opportunities for Collaborative Research at the Clinical Center (U01)
            • NIH Bench-to-Bedside Program
          • Activities with Outside Organizations
        • NIH Human Biospecimen Program
          • Frequently Asked Questions
          • List of Biospecimen Liaisons
        • Investigation of Allegations of Research Misconduct
      • NIH Guidelines
    • Authorship Guidelines and Resources
      • Authorship Resources
      • NIH IRP Authorship Conflict Resolution Policy
    • Special Research Considerations
      • Dual-Use Research
      • Policy on the Ordering or Provision of Synthetic Nucleic Acids in the IRP
      • Human Stem Cell Use
        • Human Embryonic Stem Cell (hESCs) Use
        • Induced Pluripotent Stem Cells (iPSCs) Use
        • Human Embryo Research and Cloning Prohibitions
      • Policies & Procedures for Human Fetal Tissue for Non-Transplantation Research Purposes
    • Responsible Conduct of Research Training
      • Instruction in Responsible Conduct of Research - Postdoc IRTA, CRTA, VF, Research Associates
        • Reproducibility Training
        • Introduction to “My Laboratory”
      • Instruction in Responsible Conduct of Research - Postbacs and GPP Students
      • Resources for Training Directors
      • Annual Review of Ethics (Case Studies)
        • Research Cases for Use by the NIH Community
          • 2021 Ethics Case Facilitator Training
    • Government Ethics
      • Guidelines for Non-FTEs (Trainees) for NIH-Related Activities, Outside Activities, and Awards
    • Bioethics
  • Mentoring & Training
    • Guide to Training and Mentoring
    • Guidelines for Mentors at NIH
    • Guidelines for Trainees at NIH
    • Guidelines for Annual Progress Review of Trainees
    • Scientific Director Policy Updates for Mentors and Trainees
    • Goals for Enhanced Mentoring in the IRP
    • Mentoring Cases for Discussions
  • Submitting Research Publications
    • Intramural Academic Freedom Guidance
    • Publication and Abstract Review
    • FAQs on Intramural Publication Reviews
    • NIH Publishing Agreement Forms
      • Procedures for Non-Peer-Reviewed Publications
    • PubMed Central (PMC) Deposition Requirements
    • Reproducing Figures from NIH Research Publications
  • Intramural Research Communications & Resources
    • Annual Reports and Bibliographies
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Main navigation

  • About OIR
    • OIR Leadership & Staff
    • CRISPI
    • OIR Offices
  • Sourcebook
    • Board of Scientific and Clinical Directors
    • Committees Advisory to the DDIR
    • Processes for Reviewing NIH Intramural Science
    • Intramural Program Oversight
    • Intramural Administrative Management Council
    • Personnel
    • Tenure in the NIH Intramural Research Program
    • Awards, Fellowships, & Grant Opportunities
    • Ethical Conduct
    • Mentoring & Training
    • Submitting Research Publications
    • Intramural Research Communications & Resources
  • Lectures & Events
    • Demystifying Medicine
    • WALS
    • NIH Research Festival
  • SIGs
    • SIGs by Name
    • SIGs by Scientific Focus Area
  • IRP Website
    • A premier environment where creative scientists conduct fundamental research for the betterment of human health – we are the IRP
    • Visit Website
  • The NIH Catalyst
    • A publication for and about the NIH intramural research community
    • Visit Website
  • NIDB
    • The NIH Intramural Database collects and disseminates information about research being performed in the Intramural Programs
    • Visit Website
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