UNIVERSITY OF SOUTHERN MAINE Office of Research Integrity & Outreach

Similar documents
University of Michigan Policy On Investigating Noncompliance and Animal Welfare Concerns

IACUC Policy 09: Researcher Non-Compliance

I have read this section of the Code of Ethics and agree to adhere to it. A. Affiliate - Any company which has common ownership and control

POLICY: Conflict of Interest

COMPLAINTS POLICY AND FORM OF THE PRACTICE OF DR RUDI HAYDEN (referred to as the practice )

Office of Academic Grants and Sponsored Research Financial Conflict of Interest Disclosure, Review, and Management Procedures

Family Child Care Licensing Manual (November 2016)

ACCREDITATION OPERATING PROCEDURES

Complaints Against Member Institutions BP 104 Or TRACS

BOARD OF COOPERATIVE EDUCATIONAL SERVICES SOLE SUPERVISORY DISTRICT FRANKLIN-ESSEX-HAMILTON COUNTIES MEDICAID COMPLIANCE PROGRAM CODE OF CONDUCT

Research Integrity and Policies for Handling Misconduct. Alan L. Goldin, M.D./Ph.D.

XAVIER UNIVERSITY. Financial Conflict of Interest Policy-Federal Grant Proposals

Disruptive Practitioner Policy

Provider Rights. As a network provider, you have the right to:

NETWORK POLICY & PROCEDURE Page 1 of 6 REPORTING COMPLIANCE AND HIPAA CONCERNS AND PROBLEM RESOLUTION

Regulatory Compliance Policy No. COMP-RCC 4.60 Title:

Grievances and Resident/Family Councils

NOVA SOUTHEASTERN UNIVERSITY

Center for Medicaid and State Operations/Survey and Certification Group. Promising Practices to Support the Intake of Nursing Home Complaints

ALABAMA DEPARTMENT OF MENTAL HEALTH BEHAVIOR ANALYST LICENSING BOARD DIVISION OF DEVELOPMENTAL DISABILITIES ADMINISTRATIVE CODE

FALLON TOTAL CARE. Enrollee Information

Long-Term Ombudsman Program Policies and Procedures Manual Service Chapter

USES AND DISCLOSURES OF PROTECTED HEALTH INFORMATION: HIPAA PRIVACY POLICY

MARYLAND LONG-TERM CARE OMBUDSMAN PROGRAM POLICY AND PROCEDURES MANUAL

COMPLAINTS TO THE COLLEGE OF PSYCHOLOGISTS OF ONTARIO

Section VII Provider Dispute/Appeal Procedures; Member Complaints, Grievances, and Fair Hearings

Disciplinary Action, Suspension, or Termination

UNIVERSITY OF ROCHESTER MEDICAL CENTER BILLING COMPLIANCE PLAN

Clinical Compliance Program

Research Audits PGR. Effective: 12/04/2013 Reviewed: 12/04/2015. Name of Associated Policy: Palmetto Health Administrative Research Review

HIC Standard Operating Procedure. For-Cause Audits of Human Research Studies

Texas Higher Education oordinating oard Office of General ounsel P.O. ox 12788!ustin, TX

79th OREGON LEGISLATIVE ASSEMBLY Regular Session. Enrolled. Senate Bill 58

College of American Pathologists 325 Waukegan Road, Northfield, Illinois Advancing Excellence

COMPLIANCE WITH THIS PUBLICATION IS MANDATORY

It is the Department policy to promptly and thoroughly investigate alleged misconduct involving employees.

SUPERSEDES: New CODE NO SECTION: Physician Services. SUBJECT: Disruptive Practitioner Behavior POLICY & PROCEDURE MANUAL POLICY:

2016 Hospital Conference. Objectives. The Bureau of Health Services 5/5/2016

Complaints Procedures for Schools

Sierra College ADMINISTRATIVE PROCEDURE AP 5521

OLAW Mission. OLAW Responsibilities. C.L. Davis Current Laboratory Animal Science Seminar (CLASS)

Privacy Board Standard Operating Procedures

Meeting the Obligation

UoA: Academic Quality Handbook

Complaints Handling. 27/08/2013 Version 1.0. Version No. Description Author Approval Effective Date. 1.0 Complaints. J Meredith/ D Thompson

Christopher Newport University

CHAPTER 411 DIVISION 20 ADULT PROTECTIVE SERVICES -- GENERAL

Good decision making: Investigations and threshold criteria guidance

Grants, Research and Sponsored Programs (GRASP) Compliance Program and Plan

Campus and Workplace Violence Prevention. Policy and Program

Disruptive Practitioner Policy

Professional Compliance Program Grievance Report

ANIMAL CARE & USE MANUAL

Staff member: an individual in an employment relationship with CYM or a contractor who is paid for services to CYM.

ARTICLE 27 GRIEVANCE PROCEDURE

PREVENTION OF VIOLENCE IN THE WORKPLACE

Compliance Program Updated August 2017

Section 1 Conflicts of Interest Introduction

POLICY ON PROBATION, SUSPENSION, AND DISMISSAL OF RESIDENTS/CLINICAL FELLOWS

Patient Compl p ai l n ai t n s/ s G / r G ie i vanc van es

OREGON HEALTH AUTHORITY, OFFICE OF EQUITY AND INCLUSION DIVISION 2 HEALTH CARE INTERPRETER PROGRAM

CMHC Conditions of Participation

ALABAMA MEDICAID AGENCY ADMINISTRATIVE CODE CHAPTER 560-X-45 MATERNITY CARE PROGRAM TABLE OF CONTENTS

DEPARTMENT OF HUMAN SERVICES AGING AND PEOPLE WITH DISABILITIES DIVISION OREGON ADMINISTRATIVE RULES CHAPTER 411 DIVISION 58

Complaints, Feedback and Appeals Management

Title: HIPAA PRIVACY ADMINISTRATIVE

Page 1 of 5 ADMINISTRATIVE POLICY AND PROCEDURE

COMPLIANCE PROGRAM. Our commitment to ethical conduct and compliance depends on all employees having a clear understanding of Corporate expectations.

Carrying Out a State Regulatory Program

Complaints and Suggestions for Improvement Handling Procedure

Working document QAS/ RESTRICTED September 2006

Bias Incident Response Protocol. I. Definitions

UNIVERSITY OF PITTSBURGH SCHOOL OF NURSING ACADEMIC POLICIES AND PROCEDURES FOR THE UNDERGRADUATE AND GRADUATE PROGRAMS

COMPLAINTS ESCALATION POLICY AND PROCEDURES

The Civil Air Patrol and the United States Air Force have agreed upon a new STATEMENT OF WORK FOR CIVIL AIR PATROL. Part of the new Statement of

St Brendan s College RTO 30349

Staff member: an individual in an employment relationship with CYM or a contractor who is paid for services.

The University of Edinburgh Complaint Handling Procedure

ADMINISTRATIVE PROCEDURE 408 Reporting & Investigating Workplace Violence

Chapter 14 COMPLAINTS AND GRIEVANCES. [24 CFR Part 966 Subpart B]

HEALTH PRACTITIONERS COMPETENCE ASSURANCE ACT 2003 COMPLAINTS INVESTIGATION PROCESS

COMPLAINTS UNDER THE CIVIL AIR PATROL NONDISCRIMINATION POLICY

Harassment, Sexual Misconduct and Discrimination Policy

Chapter 19 Section 3. Privacy And Security Of Protected Health Information (PHI)

Redwood Coast Regional Center Respecting Choice in the Redwood Community

Policies and Procedures for Discipline, Administrative Action and Appeals

POSITION STATEMENT. - desires to protect the public from students who are chemically impaired.

Oklahoma State University Policy and Procedures INSTITUTIONAL RADIATION SAFETY POLICY

Purdue Animal Care and Use Committee

FLORIDA DEPARTMENT OF JUVENILE JUSTICE PROCEDURE

Know the trouble spots. Identification of issues and indicators, which may give rise to actions motivated by bias, is critical to prevention efforts.

DO I NEED TO SUBMIT FOR THIS?... & OTHER FREQUENTLY ASKED QUESTIONS. March 2015 IRB Forum

National Policy Library Document

A Guide for Parents/Carers About Making a Complaint

Current Status: Active PolicyStat ID: COPY CONTRACTOR, MEDICAL STAFF, REFERRAL SOURCE AND EMPLOYEE SCREENING POLICY

SOP : Quality Assurance Inspections SCOPE RESPONSIBILITIES. APPROVAL AUTHORITY EFFECTIVE DATE May PURPOSE 2.

Minnesota Hospice Bill of Rights PER MINNESOTA STATUTES, SECTION 144A.751

CHAPTER SIX RESNET STANDARDS 600 ACCREDIATION STANDARD FOR SAMPLING PROVIDERS

PROVIDENCE HOSPITAL. Washington, D.C. SAMPLE RESIDENT CONTRACT FOR FAMILY MEDICINE

Whistleblowing Policy

Transcription:

UNIVERSITY OF SOUTHERN MAINE Office of Research Integrity & Outreach Procedure #: IACUC - 001 Date Adopted: May 5, 2017 Last Updated: Prepared By: Casey Webster, Research Compliance Administrator Reviewed By: IACUC Chair, IACUC, ORIO Procedure Title: Noncompliance 1.0 Objective: 1.1 To describe the policies and procedures the Institutional Animal Care and Use Committee (IACUC) and the Office of Research Integrity and Outreach (ORIO) follow for handling allegations of noncompliance. 2.0 General Description: 2.1 The primary responsibility of the IACUC is to ensure the humane care and use of animals. In performing that responsibility, the IACUC addresses allegations of noncompliance with federal and state regulations and institutional policies and procedures governing the conduct of research, teaching, and training involving animals. 2.2 ORIO staff, IACUC members, or IACUC consultants do not participate in alleged noncompliance reviews if they have a financial or institutional conflicting interest or are personally involved in the research. 3.0 Definitions: 3.1 Noncomplianc e is defined as conducting research in a manner that disregards or violates federal regulations or institutional policies and procedures applicable to the conduct of research involving animals. 3.2 Continuing noncompliance is a knowing, intentional, or reckless persistent failure to adhere to the laws, regulations, or policies governing animal research. The IACUC may take into consideration the volume and complexity of a researcher s activities in making the designation of continuing noncompliance. 3.3 Serious noncompliance is a failure to adhere to the laws, regulations, or policies governing animal research and which places animals at a greater risk of harm than would otherwise existed under the IACUC-approved protocol, or the Page 1 of 6

conduct of animal research without IACUC approval. 3.4Allegation is a disclosure of possible noncompliance by a respondent to the Research Compliance Administrator (RCA) by any means of communication. 3.5Complainant is a person who makes an allegation and need not be a member of the University of Southern Maine (USM) Community. 3.6Respondent is a person who is the subject of an allegation and must be a member of the USM Community at the time the alleged noncompliance occurred. 4.0 Responsibility: 4.1 Execution of SOP: IACUC Chair, IACUC Members, ORIO Staff, RCA, Investigators, and Research Assistants. 5.0 Procedure: 5.1Submission and Screening of Allegations of Noncompliance 5.1.1 Anyone may submit allegations of noncompliance involving animal research to the RCA or Assistant Provost for Research Integrity verbally or in writing. Anyone who wishes to make an anonymous allegation should follow the procedure set forth in Section 6.3 of the USM Alleged Research Misconduct Policy RCR-101. The RCA/ORIO/IACUC shall maintain confidentiality regarding the identity of the person submitting the allegation to the extent possible. 5.1.2 The RCA screens the allegation of noncompliance to determine whether the protocol(s) affected is supported by federal funds. 5.1.3 The RCA also determines whether the protocol has issues pertinent to other research review committees. 5.1.4 If the alleged violation involves a reportable disease the RCA shall notify the attending veterinarian immediately. 5.2 Preliminary Assessment of Allegation 5.2.1 The RCA reviews all allegations to determine whether the facts justify the allegation (i.e., there are supporting documents or statements). Page 2 of 6

5.2.2 If the RCA deems an allegation unjustified (i.e., finds no supporting documents or statements), the RCA communicates this determination in writing to the complainant (if the identity of the person is known) and to the investigator against whom the allegation was raised (respondent). Upon resolution of the issue, the RCA provides an oral and/or written summary of the resolution to the applicable IACUC at the next convened IACUC meeting. 5.2.3 If the RCA determines that an allegation is justified but is minor or administrative in nature, he/she manages the concern through communications with the investigator. The RCA communicates this determination in writing to the complainant (if the identity of the person is known) and to the investigator against whom the allegation was raised (respondent). Upon resolution of the issue, the RCA provides an oral and/or written summary of the resolution to the applicable IACUC at the next convened IACUC meeting. 5.2.4 If the RCA determines that an allegation is justified, the RCA forwards the allegation materials to the IACUC Chair or designee for review. The RCA shall determine an allegation is justified if, in his or her judgement: the alleged conduct could constitute Noncompliance and there is credible information to support further review. 5.2.5 If the IACUC Chair deems the allegation unjustified, the RCA communicates this determination in writing to the complainant (if the identity of the person is known) and to the investigator against whom the allegation was raised (respondent). Upon resolution of the issue, the RCA provides an oral and oral or written summary of the resolution to the applicable IACUC at the next convened IACUC meeting. 5.2.6 If the IACUC Chair determines that an allegation is justified, the RCA initiates an inquiry into an allegation. 5.3 Initiating an Inquiry into an Allegation 5.3.1 If the IACUC Chair determines that an allegation is justified, the RCA notifies the investigator. If the allegation involves co-investigator(s) or research assistant(s), the RCA also contacts these individuals (by phone, email, or letter). 5.3.2 The IACUC Chair appoints the RCA and/or designee(s) to gather information pertaining to the nature of the allegation, the procedures Page 3 of 6

approved in the IACUC protocol, and the procedures followed in conducting the study. 5.3.3 When appropriate, the RCA interviews the complainant or, in cases where the complainant requests anonymity, the individual who received the original allegation interviews the complainant. The interviewer prepares a summary of the interview and gives the complainant the opportunity to comment on the written summary. In some cases, the complainant may have already submitted a written complaint, which the RCA then verifies. The RCA may request additional information from the complainant. 5.3.4 When appropriate, the RCA interviews the respondent and gives him/her the opportunity to comment on the allegation and provide information. The RCA prepares a summary of the interview and gives the respondent the opportunity to comment on the summary. The respondent may submit a written rebuttal to the complaint, which the RCA verifies. The RCA may request additional information from the respondent. 5.3.5 Depending on the nature of the allegation and the information collected during the interviews, the RCA may interview other individuals. In addition, in conducting the review, the RCA may examine research data, both published and unpublished, the applicable approved IACUC protocol, and any other pertinent information. 5.3.6 When appropriate, the RCA prepares a summary report for the convened IACUC. The report may consist of a summary of the allegations, interview summaries, and copies of pertinent information or correspondence. The report may or may not include recommendations for IACUC action. In some cases, the RCA simply provides the convened IACUC with a summary of the allegations, the interview summaries, and copies of pertinent information without an accompanying written report. 5.4 Review Procedures 5.4.1 The RCA advises the IACUC regarding the applicable University and federal regulations, assists the IACUC in documenting the review, answers questions about the review process, maintains the records as required by state and federal laws, and serves as a liaison with the funding agency or agencies. 5.4.2 The IACUC reviews the material presented by the IACUC Page 4 of 6

representative at a convened meeting at which a quorum is present. The materials provided include the summary report of the noncompliance and the protocol if applicable. The convened IACUC determines whether to request additional information or whether to interview additional witnesses. The IACUC may give the respondent the opportunity to meet with the convened IACUC before it takes final action. 5.5 Review Outcomes/IACUC Actions 5.5.1 The convened IACUC makes the determination whether the allegation is substantiated, and if so, whether the noncompliance is serious or continuing or both based on the materials compiled during the inquiry. If the noncompliance is serious or continuing or both, the Institutional Official (IO), with the assistance of the RCA, reports the incident(s) to the applicable federal agency. 5.5.2 The convened IACUC may take a variety of actions, depending on the outcome of the review, including, but not limited to, the following: Approve continuation of research without changes; Request formal educational intervention; Request minor or major changes in the research procedures; Require the investigator create a plan of action to remedy the noncompliance; Require monitoring of research; Suspend or terminate IACUC approval/disapprove continuation of the study; Require audits of other active protocols of the investigator; Disqualify the investigator from conducting research involving animals at the University; Determine that the investigator may not use the data collected for publication; Request that the investigator inform publishers and editors if he/she has submitted or published manuscripts emanating from the research; and/or Referral to other university entities (e.g., General Counsel or Human Resources). 5.5.3 The RCA informs the following individuals of the allegation, the review process, and the findings of the review, if appropriate, depending upon the outcome of the review, the external sponsor, or the requirements of the applicable regulatory agency: Investigator; Complainant; Page 5 of 6

Research Integrity Officer; Department Chair; Dean; Human Resources; Provost; Office of Laboratory Animal Welfare; United States Department of Agriculture; Association for the Assessment and Accreditation of Laboratory Animal Care; Sponsor; and/or Other administrative personnel as appropriate. 5.5.4 The RCA resolves questions or concerns raised by an investigator regarding the outcome of a specific IACUC noncompliance review through direct communication with the investigator. 5.6 Re-evaluation/Appeal of IACUC Decisions 5.6.1 The investigator submits new information which was not part of the investigation or concerns of due process in writing to the IACUC within thirty days of the date the IACUC issues the final decision. The investigator specifies the nature of any claimed procedural error or the perceived unfairness of sanctions issued. 5.6.2 The IACUC limits concerns to a review of the procedures employed to reach the decision (i.e., claims that the process was faulty in a way that creates a considerable risk that the outcome was incorrect) or grievances against sanctions imposed as a result of a finding of noncompliance. 5.6.3 The record for the purpose of the concern raised shall be the record established during the protocol review. 6.0 References: 6.1 PHS Policy on Humane Care and Use of Laboratory Animals IV.F.3; NOT-OD-05-034 Guidance on Prompt Reporting to OLAW under the PHS policy on Humane Care and Use of Laboratory Animals; 9 CFR 2.31 (d)(7) Page 6 of 6