University Policies
Policy Contact
Senior Director, Office of Research Integrity Email (401) 863-3295

Policy on Handling Allegations of Research Misconduct

Policy No. Issue Date Effective Date
10.10.40

1.0 Policy Purpose

The purpose of this Policy on Handling Allegations of Research Misconduct (the “Research Misconduct Policy”) is to describe how Brown University (“Brown”) handles Allegation(s) of Research Misconduct. It outlines the rights and responsibilities of the parties involved in Research Misconduct reviews when Brown receives Allegation(s) of Research Misconduct.

2.0 To Whom the Policy Applies

This policy applies to all individuals involved in research at Brown, including any person involved in the review of Research Misconduct Allegations and Research Misconduct Proceedings involving Brown research paid by, under the control of, or affiliated with Brown at the time of the alleged Research Misconduct, including but not limited to scientists, trainees, technicians, other staff members, students, fellows, guest researchers, or collaborators. 

3.0 Policy Statement

Brown prohibits any form of dishonesty or misconduct in research. Brown maintains high standards of research integrity. All individuals involved in research at Brown must conduct research in a manner reflecting these standards.

Research Misconduct is a specific type of misconduct that involves Falsification, Fabrication, or Plagiarism in proposing, performing, or reviewing research, or in reporting research results. Research Misconduct does not include honest error or differences of opinion.

When an Allegation of Research Misconduct is received by the Brown Research Integrity Officer or that person’s designee (“the RIO”), the RIO will review and handle the Allegation in accordance with the procedures outlined in the Standard Operating Procedures for Handling Allegations of Research Misconduct at Brown University (the “Research Misconduct SOP”), which incorporates procedures established by regulations and policies of U.S. Federal agencies, including but not limited to the Public Health Service Policies on Research Misconduct (42 C.F.R Part 93) and the National Science Foundation Research Misconduct Policy (45 C.F.R Part 689).

Particular circumstances in an individual case, such as requirements of an external sponsor, may require a variation in procedures set forth in the Research Misconduct SOP. Any variation in those procedures must uphold the principles of the Research Misconduct SOP, including fair treatment for the subject of the Allegation.

3.1 Confidentiality

Confidentiality is a fundamental principle in Research Misconduct Proceedings. Confidentiality protects the integrity of the process.

Disclosure of the identity of Respondents, Complainants, and Witnesses during the course of a Research Misconduct Proceedings is limited to those whom Brown determines have a need to know, to execute a thorough, competent, objective, and fair Research Misconduct Proceeding. Disclosure may also be made as dictated by law, agency requirements, or court order. Those with a need to know may include institutional review boards, journals, editors, publishers, co-authors, and collaborating institutions.

Brown must disclose the identity of Respondents and Complainants, or other relevant persons, to HHS Office of Research Integrity (ORI) or other external sponsors pursuant to notification requirements under applicable federal regulations and policies, including but not limited to 42 CFR Part 93 and 45 CFR Part 689.

Except as may otherwise be prescribed by applicable law, confidentiality must be maintained for any records or Evidence from which research subjects might be identified. Inappropriate dissemination of information may result in sanctions up to and including termination.

Except as otherwise required by law, this limitation on disclosure of the identity of Respondents, Complainants, and Witnesses no longer applies once Brown has made a final determination, though Brown may continue to maintain confidentiality as circumstances warrant.

3.2 Record Retention

Brown will retain all records related to any Allegations of Research Misconduct for a minimum of seven years after the date of final determination. In cases where sponsors require longer retention periods or dictate specific retention and custody requirements, Brown must comply with those requirements. Brown may grant sponsors of the research that is the subject of a Research Misconduct Allegation or Proceeding access to the records upon the sponsor’s reasonable request and subject to any confidentiality requirements and considerations.

3.3 Notification of Sponsors

The RIO will notify a sponsor of that sponsor’s funded awards involved in Research Misconduct Proceedings in accordance with requirements set forth in the sponsor’s policies and/or award terms and conditions and the Research Misconduct SOP.

3.3.1 Notifications to Federal Sponsors

Specific notification requirements apply to Research Misconduct Proceedings when federal research funding, such as PHS, NSF, Department of Defense (DoD), or Department of Energy (DoE) funding is involved. These requirements are outlined in detail in the Research Misconduct SOP.

3.4 Institutional Administrative Actions

Brown University will take appropriate administrative or other actions related to Allegations of Research Misconduct and any Findings. The Deciding Official (“the DO”) will decide, in consultation with other institutional parties as needed, on the appropriate administrative or other actions the institution will take.

Administrative or other actions may include, but are not limited to, the following:

  • withdrawing or correcting pending or published abstracts and papers;
  • removing the responsible person for Research Misconduct from relevant projects;
  • issuing letters of reprimand to the person(s) responsible for Research Misconduct;
  • implementing special monitoring of relevant individuals’ future work;
  • placing relevant individuals on probation;
  • suspending relevant individuals;
  • removing institutional responsibilities and reducing salary accordingly;
  • initiating steps that could lead to rank reduction or termination; or
  • restoring funds to the sponsor as appropriate or required.

3.5 Using a Consortium or Other Person for Research Misconduct Proceedings/Multi- institutional Research Misconduct Proceedings/Ceding Review to Another Institution

Brown reserves the right to use the services of a committee, consortium, or person(s) that the institution determines to be reasonably qualified by practice and experience to conduct Research Misconduct Proceedings. A consortium may be a group of institutions, professional organizations, or mixed groups that will conduct Research Misconduct Proceedings for other institutions. A consortium or person involved in a Research Misconduct Proceeding being conducted by Brown must follow the requirements of this policy and the Research Misconduct SOP.

When Research Misconduct Proceedings involve multiple institutions, Brown, within its discretion,

may (a) conduct a joint Research Misconduct Proceeding, or (b) cede review to the other institution(s) through a written agreement with the other institution(s). The RIO will inform the Respondent and the Complainant, if known and appropriate, of a decision to conduct a joint proceeding or to cede review. 

When conducting a joint proceeding, one institution must be designated as the lead institution. In joint proceedings, determinations related to whether further inquiry and/or investigation is warranted, whether research misconduct occurred, and the institutional actions to be taken may be made by the institutions jointly or tasked to the lead institution. Joint proceedings may include inquiry and/or, if applicable, investigation committee members from the institution(s) involved.

When ceding review to the other institution(s), Brown must, as part of the written agreement, receive a copy of the other institution(s) final report and determination letter, and Brown’s DO may take administrative or other actions in accordance with Brown policies and procedures.

3.6 Other

3.6.1 Termination of Brown Employment or Resignation Prior to Completing Inquiry or Investigation

The termination of the Respondent's institutional employment, by resignation or otherwise, before or after an Allegation of Research Misconduct has been reported, will not preclude the start of or terminate ongoing Research Misconduct procedures. If the Respondent elects to resign from Brown prior to the initiation of the Inquiry, but after an Allegation has been made, or during an Inquiry or Investigation, the Inquiry and, if applicable, the Investigation will proceed. If the Respondent refuses to participate in the process after resignation, the committee will use its best efforts to reach a conclusion concerning the Allegation, noting in its report the Respondent’s refusal to participate and its effect on the committee’s review of all the Evidence.

3.6.2 Restoration or Protection of the Respondent's Reputation

Brown will undertake all reasonable, practical, and appropriate efforts to protect and restore the reputation of any person alleged to have engaged in Research Misconduct, but against whom no Finding of Research Misconduct was made.

If Brown finds no Research Misconduct, the Respondent may request restoration of their reputation by submitting a formal request to the RIO.  If substantiated and after consulting with the Respondent as needed, the RIO will undertake reasonable efforts to restore the Respondent’s reputation. Depending on the particular circumstances, the RIO may consider notifying those individuals aware of or involved in the Investigation of the outcome, publicizing the final outcome in forums in which the Allegation of Research Misconduct was previously publicized, or expunging all reference to the Research Misconduct from the Respondent's personnel file. Any Brown actions to restore the Respondent's reputation must first be approved by the DO in consultation with the RIO.

If a Respondent breaches the confidentiality of the Proceedings, whether intentionally or through negligence, Brown may not be able to rectify any reputational harm that may result from such a breach and may not be able to restore the Respondent’s reputation.

Brown encourages all parties to uphold confidentiality in accordance with applicable policies and ethical standards to ensure a fair and respectful process.

3.6.3 Protection of the Complainant and Others Engaged in Research Misconduct Proceedings

The RIO will make reasonable efforts to institutionally support Complainants who made Allegations of Research Misconduct in Good Faith and any individuals who participate in, or cooperate in Good Faith with, Inquiries and Investigations of such Allegations. This includes making reasonable efforts during the Research Misconduct Proceedings, including during the Inquiry and Investigation, when applicable, to prevent Retaliation against the Complainant and others engaged in Research Misconduct Proceedings, including the DO

Upon completion of a Research Misconduct Proceeding, the RIO will determine, after consulting with the Complainant as needed, what reasonable steps, if any, Brown may take to restore the position or reputation of the Complainant if such restoration is needed. The RIO, in consultation with the DO, is responsible for implementing any such steps.

If a Complainant breaches the confidentiality of the Proceedings, whether intentionally or through negligence, Brown may not be able to rectify any reputational harm that may result from such a breach and may not be able to restore the Complainant’s position and reputation.

3.6.4 Allegation(s) Not Made in Good Faith

If relevant, the RIO will determine whether the Complainant's Allegation(s) of Research Misconduct were made in Good Faith. If a determination is made that an Allegation was not made in Good Faith, the RIO will determine whether any administrative or other action should be imposed on the Complainant.

3.6.5 Interim Administrative Actions

Institutional officials will take interim administrative or other actions, as appropriate, to protect the scientific integrity and, if external funds are involved, protect external sponsors’ funds.

3.7 Research Integrity Assurance

As a recipient of PHS support for biomedical or behavioral research, training or activities related to that research or training, Brown must maintain an active Research integrity assurance with HHS ORI. Brown’s Institutional Certifying Official must assure annually on behalf of the institution that Brown

a) has written policies and procedures for addressing allegations of research misconduct, in compliance with 42 CFR Part 93;
b) complies with its policies and procedures for addressing allegations of research misconduct;
c) complies with all provisions of 42 CFR Part 93.

4.0 Definitions

For the purpose of this policy, the terms below have the following definitions:

Allegation(s):

A disclosure of possible Research Misconduct through any means of communication and brought directly to the attention of the RIO, DO, or Brown institutional official, or any HHS, NSF, or other external sponsor official. 

Complainant:

An individual who in good faith makes an Allegation(s) of Research Misconduct.

Conflict of Interest:

Within the context of a Research Misconduct Proceeding, Conflict of Interest means the real or apparent bias that may occur due to prior or existing personal or professional relationships or financial interests of those involved in the Proceeding. 

Deciding Official (DO):

The institutional official who makes final determinations on the Allegation(s) of Research Misconduct after the review of the report of the person(s) conducting the Inquiry and, if applicable, Investigation Committee, and any recommended institutional administrative actions. The Vice President for Research (VPR) serves as the DO.

Evidence:

Anything offered or obtained during a Research Misconduct Proceeding that tends to prove or disprove the existence of an alleged fact. Evidence includes documents, whether in hard copy or electronic form, information, tangible items, and testimony.

Fabrication:

Making up data or results and recording or reporting them.

Falsification:

Manipulating research materials, equipment, or processes, or changing or omitting data or results such that the research is not accurately represented in the Research Record.

Finding(s):

A finding of Research Misconduct requires that: (a) There be a significant departure from accepted practices of the relevant research community; and (b) The misconduct be committed intentionally (i.e., acting with the aim of carrying out this act), knowingly (i.e., acting with the awareness of the act), or recklessly (i.e., proposing, performing, or reviewing research with indifference to known risks of fabrication, falsification, or plagiarism); and (c) The Allegation(s) be proven by a preponderance of the Evidence. Preponderance of the Evidence means proof by Evidence that, compared with Evidence opposing it, leads to the conclusion that the fact at issue is more likely true than not.

Good Faith:

As applied to a Complainant, means having a belief in the truth of one's Allegation(s) or testimony that a reasonable person in the Complainant's position could have based on the information known to the Complainant at the time. Allegation(s) or testimony are not in Good Faith if made with knowing or reckless disregard for the truth or for information that would negate the Allegation(s).  Good Faith, as applied to an Inquiry or Investigation committee member, means cooperating with the Research Misconduct Proceeding by carrying out the duties assigned impartially for the purpose of helping an institution meet its responsibilities under this Policy and the associated Standard Operating Procedures for Handling Allegations of Research Misconduct. 

HHS Office of Research Integrity (ORI):

The office established by Public Health Service Act section 493 (42 U.S.C. 289b) and to which the HHS Secretary has delegated responsibility for addressing research integrity and misconduct issues related to PHS-supported activities (defined as PHS funding, or applications or proposals for PHS funding, for biomedical or behavioral research, biomedical or behavioral research training, or activities related to that research or training, that may be provided through funding for PHS intramural research; PHS grants, cooperative agreements, or contracts; subawards, contracts, or subcontracts under those PHS funding instruments; or salary or other payments under PHS grants, cooperative agreements, or contracts).

Inquiry:

Preliminary information gathering and preliminary fact-finding to determine whether Allegation(s) or apparent instances of Research Misconduct warrant an Investigation.

Institutional Certifying Official:

The institutional official at Brown who is responsible for assuring on behalf of the institution that Brown has written policies and procedures for addressing allegations of research misconduct, in compliance with 42 CFR Part 93; and complies with its policies and procedures and the requirements of 42 CFR Part 93. The Institutional Certifying Official is responsible for certifying the content of Brown’s annual report to HHS ORI.

Investigation:

The formal development of a factual record and the examination of that record leading to a decision not to make a Finding of Research Misconduct or to a recommendation for a Finding of Research Misconduct which may include a recommendation for other appropriate actions, including administrative actions.

PHS:

The U.S. Public Health Service, an operating component of the Department of Health and Human Services (DHHS).

Plagiarism:

The appropriation of another person’s ideas, processes, results, or words, without giving appropriate credit. Plagiarism includes the unattributed verbatim or nearly verbatim copying of sentences and paragraphs from another’s work that materially misleads the reader regarding the contributions of the author. It does not include the limited use of identical or nearly identical phrases that describe a commonly used methodology. Plagiarism does not include self-plagiarism or authorship or credit disputes, including disputes among former collaborators who participated jointly in the development or conduct of a research project. Self-plagiarism and authorship disputes do not meet the definition of Research Misconduct.

Research Integrity Officer (RIO):

The institutional official responsible for assessing Allegation(s) of Research Misconduct and determining when such Allegation(s) warrant inquiries and for overseeing inquiries and Investigations. The Senior Director of Research Integrity, or the Senior Director’s designee, serves as the RIO, and is appointed by the Vice President for Research.

Research Misconduct:

Fabrication, falsification, or plagiarism in proposing, performing, or reviewing research, or in reporting research results. Research misconduct does not include honest error or differences of opinion.

Research Misconduct Proceeding:

Any actions related to alleged Research Misconduct including Allegation Assessments, Inquiries, or Investigations.

Research Record:

The record of data or results that embody the facts resulting from scientific inquiry. Data or results may be in physical or electronic form. Examples of items, materials, or information that may be considered part of the research record include, but are not limited to, research proposals, raw data, processed data, clinical research records, laboratory records, study records, laboratory notebooks, progress reports, manuscripts, abstracts, theses, records of oral presentations, online content, lab meeting reports and journal articles.

Respondent:

The individual against whom the Allegation(s) of Research Misconduct are directed or the person whose actions are the subject of the Inquiry or Investigation. There can be more than one Respondent in any Inquiry or Investigation.

Retaliation:

Any adverse action taken against anyone engaged in a Research Misconduct Proceeding by an institution or one of its members in response to: (a) a Good Faith Allegation of Research Misconduct or (b) Good Faith cooperation with a Research Misconduct Proceeding.

Witness:

Any person whom the RIO has engaged on behalf of the Inquiry and/or Investigation Committee to provide expertise, Evidence, or testimony related to a potential Research Misconduct. The Complainant and/or Respondent may identify potential Witnesses to the RIO and request that they be interviewed by the relevant committee.

5.0 Responsibilities

All individuals to whom this policy applies are responsible for becoming familiar with and following this policy. University supervisors and employees with student oversight duties are responsible for promoting the understanding of this policy and for taking appropriate steps to help ensure and enforce compliance with it.

Brown Employees and Individuals Associated with Brown: All employees or individuals associated with Brown University have a responsibility to report observed, suspected, or apparent Research Misconduct involving Brown community members or Brown research to the RIO. Any individual who is unsure whether a suspected incident falls within the definition of Research Misconduct may contact the RIO to discuss the suspected Research Misconduct without making a formal Allegation. If the circumstances do not meet the definition of Research Misconduct but fall under different policies, the RIO will refer the individual or Allegation(s) to other offices or officials with responsibility for those policies.

Brown Employees: Brown employees must reasonably cooperate with the RIO and other University officials in the review of Allegation(s) and the conduct of Inquiries and Investigations. Employees have an obligation to preserve and provide relevant Evidence related to Research Misconduct Proceeding to the RIO or other institutional officials officially engaged in an Inquiry or Investigation.

Research Integrity Officer: The RIO has primary responsibility for implementation of this policy and the Research Misconduct SOP, as well as any other related procedures. If the RIO has an actual or perceived Conflict of Interest related to a particular Research Misconduct matter, Brown must mitigate that Conflict of Interest, which mitigation may include appointing another appropriate individual to serve as RIO for that matter.

In addition to the responsibilities outlined in the policy, the RIO will:

  • take reasonable and practical steps to identify Research Records and Evidence needed to conduct the Research Misconduct Proceeding, inventory the records and Evidence, and sequester them in a secure manner.
  • appoint the person(s) conducting the Inquiry and, if applicable, Investigation and ensure that necessary and appropriate expertise is available to carry out a thorough and authoritative evaluation of the relevant Evidence in an Inquiry or Investigation.
  • maintain confidentiality as appropriate and required by this policy, applicable law and regulations, and otherwise required or expected.
  • assist during the Inquiry and Investigation and support  institutional personnel in complying with this policy, related procedures, and applicable standards imposed by government or external funding sources.
  • keep the DO and others with a need to know apprised of the progress of the Research Misconduct Proceeding.
  • be responsible for securing and maintaining the confidentiality of all documents and Evidence.
  • take appropriate or required action to notify other involved parties, such as sponsors, law enforcement agencies, professional societies, and licensing boards, of those actions.
  • report relevant information to external sponsor(s) of implicated research, as required by regulation.

Deciding Official: The DO has primary authority for making decisions about Research Misconduct, including making a Finding, after considering the reports and recommendations from the Inquiry and, if applicable, Investigation. If the DO has an actual or perceived Conflict of Interest related to a particular Research Misconduct matter, Brown must mitigate that Conflict of Interest, which mitigation may include appointing another appropriate individual to serve as DO for that matter.

The DO will:

  • review the final Inquiry and/or Investigation report, the recommendations of the Inquiry or Investigation committee, and any written comments made by the Respondent on the draft report(s).
  • decide whether to conduct an Investigation.
  • after the conclusion of an Investigation, determine whether Research Misconduct occurred, and whether to impose sanctions or take other appropriate action(s), including administrative actions.
  • coordinate with relevant institutional officials to confirm that the findings of the DO, as well as the final Investigation report and a description of any pending or completed administrative actions, are provided to any sponsor(s) as required or appropriate.

Complainant: The Complainant may have an opportunity to testify during  the Inquiry and Investigation and be informed of the results of the Inquiry and Investigation. The Complainant is responsible for making Allegation(s) in Good Faith and cooperating, in Good Faith, with an Inquiry or Investigation.

Respondent: The Respondent is responsible for cooperating with the conduct of an Inquiry or Investigation. The Respondent will have the opportunity to be interviewed by and present Evidence during the Inquiry and Investigation, to review the draft Inquiry and Investigation reports, and to have the advice of counsel. 

6.0 Consequences for Violating this Policy

Failure to comply with this and related policies is subject to disciplinary action, up to and including suspension without pay, or termination of employment or association with the University, in accordance with applicable (e.g., staff, faculty, student) disciplinary procedures.

7.0 Related Information

Brown is a community in which individuals are encouraged to share concerns with University leadership. Additionally, Brown’s Anonymous Reporting Hotline allows anonymous and confidential reporting on matters of concern online or by phone (877-318-9184).

The following information complements and supplements this document. The information is intended to help explain this policy and is not an all-inclusive list of policies, procedures, laws and requirements.

7.2 Related Procedures

  • Procedures for Handling Allegation(s) of Research Misconduct

7.3 Related Forms

N/A

7.4 Frequently Asked Questions

N/A

7.5 Other Related Information

N/A

Policy Owner and Contact(s)

Policy Owner: Vice President for Research

Policy Approved by: Vice President for Research

Contact Information:

Senior Director, Office of Research Integrity Email (401) 863-3295

Policy History

Policy Issue Date:

Policy Effective Date:

Policy Update/Review Summary:

Previous policy version(s) superseded by this policy:

  • Policy on Handling Allegations of Research Misconduct, Effective Date: May 9, 2025
  • Policy on Handling Allegations of Research Misconduct, Last Updated: August 15, 2017