Office of Research Oversight 1 ORO Research Suspensions and Other ACOS/R Concerns Tom Puglisi, PhD Local Accountability in Research April 8, 2010.

Slides:



Advertisements
Similar presentations
The Role of the IRB An Institutional Review Board (IRB) is a review committee established to help protect the rights and welfare of human research subjects.
Advertisements

What FDA Looks for When Inspecting IRBs and Sponsors Marian J. Serge Nurse Consultant Division of Bioresearch Monitoring Office of Compliance Center for.
Tips to a Successful Monitoring Visit
Gerald Treiman, IRB Chair John Stillman, IRB Director Maureen Brinkman, IRB Administrator Ann Johnson, IRB Administrator.
Suzanne Reister, Program Manager Paula Vanderpool, Program Assistant North Central Washington Workers’ Comp Trust Chemical Hygiene – Hazardous Chemicals.
Office of Research Oversight. Working Group Report Slide 2.
IRB Determinations 1. AAHRPP Site Visit Results Site visitors observed a real commitment to human subject protections Investigator and research staff.
Unit 1. Lab Safety video I TO PREVENT: __________________________________________ __________________________________________ exposure to __________________________________________.
CSHEMA 2007, BOSTON, MA CLIP AT UNC CHAPEL HILL-TEN YEARS LATER Collaborative Laboratory Inspection Program at UNC Chapel Hill-Ten Years Later Jonathan.
How to Prepare for a FTCA Site Visit Office Hours
Pharmacists Responsibilities in Clinical Studies Mike R Sather, PhD Crystal L Harris, PharmD February 26, 2004.
Office of the Campus Veterinarian Preparing Your Lab for an IACUC or AAALAC Inspection.
Collaborative Laboratory Safety Inspections (CLIP) at the University of North Carolina at Chapel Hill Jonathan Moore, Associate Radiation Safety Officer.
LABORATORY SAFETY Presented by The Office of Risk Management Loss Prevention.
Office of Research Oversight VHA Handbook Research Conducted by VHA Program Office Employees Effective May 1, 2012 October 28, 2011.
Responsible CarE® Employee health and Safety Code David Sandidge Director, Responsible Care American Chemistry Council June 2010.
Developing a Chemical Risk Management Program
Brookhaven Science Associates U.S. Department of Energy 1 Brookhaven National Laboratory Protocol Compliance Monitoring Darcy Mallon May 7, 2009.
Clinical Pharmacy’s Role in Research Trials Sheree Miller Pharm.D. Investigational Drug Service University of Washington Medical Center.
A Review of the Public Health Service (PHS) Policy on Humane Care and Use of Laboratory Animals Created by Marc S. Hulin, DVM, Dipl. ACLAM.
Unlocking the Mystery of General Information Reporting Research Compliance Administration Training Presentation Wednesday, June 6, 2007 Presenter:Heather.
Is this Research? Exempt? Expedited?
Caring for Research Animals
Sandia is a multi-program laboratory operated by Sandia Corporation, a Lockheed Martin Company, for the United States Department of Energy’s National Nuclear.
NC A&T STATE UNIVERSITY
Research and Development Protocol Submission and Continuing Review Processes Kimberly Summers, PharmD Assistant Chief for Clinical Research South Texas.
Responsible Conduct of Research (RCR) Farida Lada October 16, 2013
Elements of Clinical Trial Quality Assurance Regulatory Coordinator –SCTR SUCCESS Center QA Monitor – NIDA Clinical Trials Network Stephanie Gentilin,
ORO Reviews: Frequent Findings Related to IRBs Bob Brooks Associate Director Research Compliance Education and Policy VHA Office of Research Oversight.
Office of Research Oversight Office of Research Oversight 1 ORD Local Accountability Meetings 2007 – 2008 Tom Puglisi, PhD, CIP Joan P. Porter, MSc, DPA,
RESCUE: ACRIN 4701 Protocol Development & Regulatory Compliance (PDRC) Josephine Schloesser, ACRIN Monitor Chris Steward, ACRIN QC Auditor.
Michelle Groy Johnson Quality Improvement Officer Research Integrity Office Tough Love: Understanding the Purpose and Processes of Quality Assurance.
1 KRA Research Compliance Kuali Days VI Presenters: Lori Schultz, University of Arizona E. Ray Stinson, Ph.D., Cornell University May 14, 2008.
Safety organization and training. The biosafety officer and biosafety committee A safety policy, A safety manual, and Supporting programmes for their.
Use of Animals in Research: IACUC's, Animal Care Requirements and More Panel members: William Ray Stricklin, PhD IACUC Chair Douglas Powell, DVM, ACLAM.
ORO Reviews: Frequent Findings Bob Brooks Associate Director Research Compliance Education and Policy VHA Office of Research Oversight May, 2012.
Research Compliance: An Overview of the Players and Issues Involved in Emory’s Research Compliance Programs.
TERRENCE F. ACKERMAN, PH.D. PROFESSOR OF BIOETHICS CHAIR, UTHSC IRB.
OSU-CHS ALARA Statement The OSU-CHS radiation safety program will be conducted in such a manner so that exposure to faculty, staff, students, the public,
VHA Handbook “Research Compliance Reporting Requirements” Version: June 15, 2015 ORO Presentation: July 14 and 16, 2015.
Investigators’ Responsibilities in Conducting Human Subjects Research Dept. of Regulatory Affairs April 18, 2012.
DOMESTIC AND FOREIGN SUBCONTRACTS/SUBAWARDS CITI Training.
Conducting Clinical Risk Assessments And Implementing Compliance Practices Jane L. Stratton Chiron Corporation VP/Associate General Counsel Chief Compliance.
Office of Research & Development (ORD) Local Accountability of Research 2009 Baltimore, Maryland January 13-14, 2009 “Meeting the Current Challenges of.
AUDIT REQUIREMENTS, FINDINGS & BASICS RESEARCH COMPLIANCE.
Office of Research Oversight 1 VHA Handbook Research Compliance Reporting Requirements HRPP September
Division of Risk Management State of Florida Loss Prevention Program.
Institutional Review Board Issues for Classroom Research Sharon McWhorter IRB Administrator, The University of Akron (With assistance from Phil Allen,
Deona Willes, Basic Steps for New LabsBasic Steps for New Labs  Complete forms for protocol review and submit chemical inventory.
OBSERVED IN ORO REVIEWS COMPLIANCE ISSUES: OBSERVED IN ORO REVIEWS David A. Weber, Ph.D., FACNP Acting Chief Officer Office of Research.
Animals in Research Donald B. Casebolt Director, Department of Animal Resources.
VHA Research Compliance Reporting Requirements ORD Accreditation Conference Call December 15, 2011.
Office of Research Oversight 1 Core Responsibilities for Human Research Protection Research Compliance Officers Robert Brooks, MD, PhD, MBA Associate Director,
LOUISIANA STATE UNIVERSITY HEALTH SCIENCES CENTER NEW ORLEANS.
Office of Research Oversight 1 Office of Research and Development Local Accountability Meeting January 2009.
Paul Kelly Facility Research Compliance Officer for the Ralph H. Johnson VA Medical Center.
Office of Human Research Protection Georgia Health Sciences University.
Durham VA Medical Center Animal Research Program Lessons Learned.
WISHA, 7/23/04 Employee Medical and Exposure Records Chapter WAC Employer Responsibilities.
Office of Research & Development (ORD) Local Accountability of Research 2009 Baltimore, Maryland January 13-14, 2009 “Meeting the Current Challenges of.
Office of Research Oversight What’s New in VHA Handbook Dated November 15, 2011 December 1, 2011.
VA Central IRB K. Lynn Cates, MD Assistant Chief Research & Development Officer Office of Research & Development Department of Veterans Affairs.
VA Central IRB K. Lynn Cates, MD Assistant Chief Research & Development Officer Office of Research & Development Department of Veterans Affairs September.
CONDUCTING COMPLIANCE ASSESSMENTS Allen Ditch Director Corporate Quality Bristol Myers Squibb Medical Research Summit March 6, 2003.
Survey of IACUC Administrative Staff. Survey Results 2005 – 132 Respondents 2012 – 63 Respondents.
Protocol Violations and Protecting Animal Subjects Patricia Brown, VMD, MS, DACLAM Director, Office of Laboratory Animal Welfare National Institutes of.
Supervisory Responsibilities of Clinical Investigators
NC A&T STATE UNIVERSITY
Reportable Events & Other IRB Updates February 2017
Chemical Safety and Security Plan
Presentation transcript:

Office of Research Oversight 1 ORO Research Suspensions and Other ACOS/R Concerns Tom Puglisi, PhD Local Accountability in Research April 8, 2010

Office of Research Oversight 2 ORO Criteria for Suspension of Research Substantive concerns about : The safety, rights, or welfare of human subjects, research personnel, or others The safety, health, or welfare of laboratory animals The effectiveness of a facility’s research protection or research oversight programs

Office of Research Oversight 3 ORO Research Suspensions (2006 – 2010) Multi-Site Programs or Projects: REAP (Research Enhancement Award Program) Projects –Information security and confidentiality protections Smoking Cessation Study –Subjects and providers not informed about research on 4 different intervention approaches assigned solely by site location –Providers not alerted to use of bupropion and risks/contraindications Varenicline (Chantix) – –Safety monitoring –Notification of subjects and providers concerning risks Nursing Management Implementation Study –On-site interview of VA personnel without local IRB approval

Office of Research Oversight 4 ORO Research Suspensions (2006 – 2010) Facility Programs: All Research (3 Facilities) Programmatic Lack of Management Controls / Infrastructure Facility could not identify all VA research projects Widely discrepant protocol inventories (ie, R&DC vs IRB or IACUC or SRS) Systematic lack of R&DC review and/or approval Inability to track project approval and expiration dates Systematic lack of documentation (ie, Research Service did not maintain protocol files)

Office of Research Oversight 5 ORO Research Suspensions (2006 – 2010) Facility Programs: Human Research (1 Facility) Affiliate IRB Chair and members lacked basic knowledge of Common Rule, FDA, and VA requirements IRB ignored audit findings of serious noncompliance Inadequate IRB review and oversight of research resulting in FDA suspensions Research Service lacked protocol records, tracking, etc Lack of Conflict of Interest review procedures Lack of procedures to verify credentialing and privileging Lack of procedures to verify investigator training

Office of Research Oversight 6 ORO Research Suspensions (2006 – 2010) Facility Programs: Animal Research (2 Facilities) Facility 1: Withdrawal of Affiliate from AAALAC Program Facility 2: Systematic failure of ACUP Oversight Program –IACUC Chair and members lacked basic knowledge of PHS Policy, UDSA, and VA requirements –Failure to complete and/or follow-up on Semi-Annual Program Reviews and Facility Assessments –Lack of Researcher Occupational Safety & Health Program –VMO lacked control over animal procurement and intake –VMO lacked access to ACORPs and animal laboratories –Lack of mechanism to track animal census and link to protocols

Office of Research Oversight 7 ORO Research Suspensions (2006 – 2010) Facility Programs: Animal Research (2 Facilities) Facility 2: Systematic failure of ACUP Oversight Program –Lack of population management mechanisms –Controlled substances acquired outside VA –Controlled substances stored in unlocked cabinets –Widespread use of non-pharmaceutical grade and/or expired drugs –Widespread violations of animal surgery standards –Lack of HVAC and cage wash temperature monitoring –Lack of primate technician and primate enrichment program –Chronic animal infection problems –Lack of mechanism to ensure training prior to handling animals –Multiple safety deficiencies

Office of Research Oversight 8 ORO Research Suspensions (2006 – 2010) Facility Programs: Research Safety (3 Facilities) Facility 1: BSL-3 Lab Suspension –Inappropriate transfer of hazardous material –Possible loss of hazardous material –Inadequate material inventory procedures Facility 2: Failure to Conduct Individual Protocol Reviews Facility 3: Systemic Failure of Safety Oversight Program –Widespread unsafe chemical storage –Multiple inoperative eye wash stations –Use of Bunsen burners in unsuited biosafety cabinets

Office of Research Oversight 9 ORO Research Suspensions (2006 – 2010) Facility Programs: Research Safety (2 Facilities) Facility 3: Systemic Failure of Safety Oversight Program –Improper/dated inspections of biosafety cabinets and fume hoods –Outdated chemical inventories –Multiple longstanding fire code violations –Failure to label equipment, supplies, and waste as radioactive –Failure to decontaminate abandoned laboratories –Lack of Researcher Occupational Safety & Health Program –Lack of training and supervision of laboratory personnel –Failure to correct chronic deficiencies

Office of Research Oversight 10 On-Site Program Reviews – Routine Inspections, Follow-Up Inspections, For-Cause Reviews (Human, Animal, Safety, BSL-3, Information Protection, R&D Oversight) CY03 CY04 CY05 CY06 CY07 CY08 CY Since 2006: 331 Program Reviews 9 Programmatic Suspensions

Office of Research Oversight 11 Deficiencies Identified – CY 2009 ORO Routine Inspections at 26 Facilities Area of Deficiency – Lack of...Percent 1.Research and Development Committee (R&DC) oversight, including annual program reviews 2.Documentation and tracking of required training, credentialing, privileging, and scope of practice 3.Effective and timely communication between affiliate Research Review Committee and VA Research Service 4.Protocol inventory controls, effective protocol tracking, and timely continuing reviews 5.Information Security Officer (ISO), and Privacy Officer protocol reviews 6.Timely reporting of adverse events and problems to ORO 7.Active involvement of Facility Leadership 65% 58% 46% 35% 27%

Office of Research Oversight 12 ORO Research Suspension and Other ACOS/R Concerns Tom Puglisi, PhD