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Marianne M. Elliott

Marianne M. Elliott. Office of Research Integrity and Ethics Bureau of Medicine and Surgery U. S Navy. Research Compliance Audit aka Monitoring Research Integrity. Concurrent Session 4.02 Friday, April 23, 2004 Marianne M. Elliott, M.S., C. I. P.

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Marianne M. Elliott

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  1. Marianne M. Elliott Office of Research Integrity and Ethics Bureau of Medicine and Surgery U. S Navy

  2. Research Compliance AuditakaMonitoring Research Integrity Concurrent Session 4.02 Friday, April 23, 2004 Marianne M. Elliott, M.S., C. I. P. Director, Clinical Investigation & Responsible Conduct of Research Programs Office of Research Integrity and Ethics, U. S. Navy

  3. Disclaimer: The opinions expressed in this presentation are solely those of the author and do not reflect the official position or views of the United States Navy, the Department of Defense or the U. S. Government.

  4. Objectives: Monitoring Research Integrity • Describe monitoring and the basis for monitoring research integrity in HRPP • Describe dimensions of monitoring in HRPP • Provide suggestions for practical approach

  5. What is monitoring? • What do you say you do? written policies & procedures • What do you do? verify actual practice • How well do you do it? evaluate, assess & improve

  6. Basis for Monitoring Research Integrity • Ethical Principles • Regulations Common Rule – Federal Policy FDA • Continuous Quality Improvement through Self Assessment • Accreditation standards • Institutional policy & procedure

  7. Basis for Monitoring Research Integrity Ethical Principles from The Belmont Report Respect for Persons Beneficence Justice

  8. Basis for Monitoring Research Integrity Common Rule *.109(e) – IRB shall conduct continuing review… authority to observe or have third party observe the consent process and the research *.111(a)(6) – When appropriate, the research plan makes adequate provisions for monitoring the data collected to ensure the safety of subjects

  9. Basis for Monitoring Research Integrity Continuous Quality Improvement through Self-Assessment • FDA model • VA model • HHS- OHRP model • Navy model • Business model

  10. Dimensions of Monitoring Research Integrity • Investigator – Protocol • IRB as part of HRPP • IRB operations/office • Institutional HRPP - integration

  11. Monitoring Research Integrity – Investigator-Protocol Research protocol includes: • post approval monitoring plan procedure for unanticipated problems & adverse events • consent process & documentation • eligibility, inclusion/exclusion criteria • data verification – accuracy, safety

  12. Monitoring Research Integrity – Investigator-Protocol Define & describe post approval monitoring plan • Investigator as sole monitor • Research team as monitor • Medical monitor • Data Monitoring Committee (DMC) or DSMB • Independent Committee – protocol unique

  13. Monitoring Research Integrity – IRB as part of HRPP IRB policy for reviewing research protocols: • Address ethical principles • Meet or exceed regulatory requirements • Approve protocol with post approval monitoring plan • Determine frequency of continuing review • Document review & decisions • Observe consent process and research

  14. Monitoring Research Integrity – IRB as part of HRPP Monitoring the IRB • Observe IRB ‘in action’ - meeting • Review documentation of decisions/actions IRB meeting minutes, review guides • Verify decisions/actions planned appropriate? implemented? • Evaluate decisions/actions – standards met?

  15. Monitoring Research Integrity – IRB office IRB Office & staff • Role & responsibilities • Staff qualifications & numbers • Pre-review – ethical principles, regulatory requirements • Investigator education – 1 by 1 • Document decisions/actions • Process flow & efficiency

  16. Monitoring Research Integrity – IRB office IRB Office & staff • Observe IRB office ‘in action’ • Review documentation of pre-review decisions/actions protocol records, review guides • Verify decisions/actions planned appropriate? implemented? • Evaluate decisions/actions – standards met? • Track actual work flow

  17. Monitoring Research Integrity – Institution’s HRPP Institution • Create culture of research integrity • HRPP structure & authority • Organizational roles & responsibilities • Communication amongst components • Education program – all levels

  18. Monitoring Research Integrity – Institution’s HRPP Institution • Observe institution ‘in action’ administration & key leader public relations, community outreach • Process & documentation of decisions/actions complaints, allegations, • Verify decisions/actions planned appropriate? implemented? • Evaluate decisions/actions – standards met?

  19. So, what is monitoring research integrity? • What do you say you do? • What do you do? • How well do you do it? Coming full circle while connecting the dots….

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