Skip to main content
v2026.1714 entries · CC-BY 4.0
CASRAI

Editorial · CASRAI

Procedure for the Investigation of Misconduct in Research: A Step-by-Step Committee Guide

A practical, UKRIO- and ORI-aligned procedure for institutional committees: intake, inquiry, formal investigation and reporting phases explained.

ByMCP Service
Published 2 Jul 2026· 6 minute read

When a university receives a formal allegation of research misconduct, the committee handling it needs a defensible, evidence-based procedure for the investigation of misconduct in research — not an improvised process assembled under pressure. UK institutions have historically anchored their local policies to the UK Research Integrity Office (UKRIO) template procedure, most recently revised in 2023. That document has now been sunset: UKRIO published a replacement, the Detailed Procedure for Investigating Breaches of Research Integrity, in December 2025, alongside long-standing US practice codified by the Office of Research Integrity (ORI). This guide synthesises both models into one practical procedure — covering intake, inquiry, formal investigation and reporting — that institutional committees can apply directly.

What Counts as Research Misconduct

Most frameworks converge on a common core: fabrication, falsification and plagiarism (FFP). ORI applies this narrow FFP definition when it proposes federal findings against researchers funded by the US Public Health Service. UK practice, shaped by the Concordat to Support Research Integrity (Universities UK), is broader.

UK institutional policies typically also capture:

  • Mismanagement of conflicts of interest that were not properly declared
  • Breach of duty of care to research participants, patients or animals
  • Misrepresentation of involvement, including ghost or guest authorship
  • Improper handling of a misconduct allegation itself, including victimising a whistleblower

Committees should confirm which definition their institutional policy uses before opening a case. Scope decisions made at intake determine whether a matter proceeds as misconduct, as poor research practice, or as a contributorship dispute better resolved through clearer role attribution.

The Procedure at a Glance: Four Phases from Intake to Report

Institutional procedures differ in their exact labels but converge on the same underlying logic. The table below maps UKRIO terminology against the ORI model used across US federally funded research.

Generic phase UKRIO term ORI (US) term Core purpose
1. Intake Receipt of Allegations Allegation Log the complaint and confirm it falls within scope and jurisdiction
2. Screening Assessment Inquiry Establish whether there is a prima facie case warranting full investigation
3. Formal investigation Investigation Investigation Panel-led evidentiary examination, typically with an external member
4. Outcome Outcome / Report Investigation Report / adjudication Findings, sanctions and correction of the research record
5. Appeal Appeal (institution-specific) Institutional and federal oversight review Review of process fairness and proportionality of any sanction

Step-by-Step: Running Each Phase

The sequence below reflects UKRIO’s revised phase structure and ORI’s assessment-inquiry-investigation model, condensed into a working checklist committees can follow.

Phase 1: Intake and Initial Screening

The designated Research Integrity Officer or Named Person logs the allegation in writing, confirms it concerns research conducted under the institution’s auspices, and checks it is not vexatious, out of time, or already covered by another process such as a student misconduct or HR grievance procedure. Both the respondent and complainant are typically notified that a review has opened.

Phase 2: The Inquiry (Preliminary Assessment)

A small screening panel gathers initial evidence — underlying data, correspondence, relevant publications — to decide whether a prima facie case exists. This is a fact-finding exercise, not a determination of guilt. Many cases close here because the conduct reflects honest error or a legitimate difference of scientific opinion rather than misconduct.

Phase 3: The Formal Investigation

If the inquiry finds sufficient grounds, a Formal Investigation Panel is convened, usually including at least one member external to the institution. The panel interviews the complainant, respondent and witnesses, scrutinises data and lab records, and applies the balance-of-probabilities standard used across UK and most US institutional procedures.

Phase 4: Outcome, Reporting and Correcting the Record

The panel issues a written report: allegations upheld, partially upheld, or not upheld. Where misconduct is confirmed, action can include disciplinary sanctions, retraction or correction of affected publications, and notification of co-authors, journals, funders and, where relevant, professional or regulatory bodies.

Phase 5: Appeal

Most institutions allow an appeal limited to procedural irregularity, new evidence, or disproportionate sanction, heard by a senior figure with no prior involvement in the case. The appeal outcome is normally final at institutional level, though funders such as UKRI may separately review an institution’s handling of a case tied to their funding.

Answer-First: Committee FAQs

What are the phases of a research misconduct allegation?

Most procedures run through four to five phases: intake (logging and scoping the allegation), inquiry or assessment (checking for a prima facie case), formal investigation (panel-led evidence review), and outcome and reporting, followed by an optional appeal stage.

What is the first phase in response to a research misconduct allegation?

The first phase is intake, sometimes called Receipt of Allegations. A designated Research Integrity Officer logs the complaint in writing, confirms it falls within the institution’s jurisdiction and definition of misconduct, and notifies the respondent before any evidence review begins.

Who investigates allegations of research misconduct?

The employing or funding institution investigates in the first instance, usually through a Formal Investigation Panel including an external member. Bodies such as UKRIO and ORI provide advice and procedural frameworks but do not typically run individual case investigations themselves.

Whose responsibility is it to identify and report research misconduct?

Reporting is a shared duty. Principal investigators, co-authors, reviewers, students and professional staff must raise good-faith concerns, usually to a named Research Integrity Officer. Institutional policies typically protect whistleblowers from retaliation once a concern is raised honestly.

Roles, Prevention and Governance Implications

Investigation procedures are remedial — they respond after harm has occurred. Prevention is cheaper and protects institutional reputation long before a case reaches a panel. Evidence-based measures include mandatory research integrity training at induction and supervision milestones, data management plans reviewed at project setup, and clear contributor-role disclosure on every output.

Authorship disputes are a recurring trigger for misconduct allegations. Transparent attribution of who did what — using a structured framework such as the CRediT contributor role taxonomy, which CASRAI originated in 2014 and which is now stewarded by NISO as ANSI/NISO Z39.104-2022 — reduces the ambiguity that often escalates into a formal complaint. Institutions embedding role transparency into their research administration workflows give committees clearer evidence to work with if a dispute does arise.

The governance stakes are rising. UKRI’s April 2025 guidance for research organisations ties funder confidence directly to the robustness of an institution’s misconduct procedure, and poorly documented cases increasingly surface in funder audits and, where publications are affected, in retraction and correction notices tracked by services such as Retraction Watch. Committees that document each phase properly do more than defend individual decisions on appeal — they protect the institution’s standing with funders and publishers.

Looking ahead, expect UKRIO’s December 2025 Detailed Procedure and equivalent US federal guidance to keep converging on shared definitions, external panel membership and proportionate, documented outcomes. Institutions that update their local policy to reference the current UKRIO and ORI models now, rather than after their next case, will be better placed to run a fair, defensible investigation when an allegation lands.

LAC

Partner Deal

LAC Health Supplies Mobile App

Referenced across the research world

University of Cambridge logoColumbia University logoUniversity of Edinburgh logoHarvard University logoUniversity of Oxford logoPrinceton University logoStanford School of Medicine logoUniversity College London logoORCID logoCrossref logoUniversity of Cambridge logoColumbia University logoUniversity of Edinburgh logoHarvard University logoUniversity of Oxford logoPrinceton University logoStanford School of Medicine logoUniversity College London logoORCID logoCrossref logo
  • University of Cambridge logo
  • Columbia University logo
  • University of Edinburgh logo
  • Harvard University logo
  • University of Oxford logo
  • Princeton University logo
  • Stanford School of Medicine logo
  • University College London logo
  • ORCID logo
  • Crossref logo

View CASRAI adoption →