The role of a research administration program in adverse event reporting

The reporting, analysis, and management of adverse events (AEs) provide an ongoing assessment of risk in the context of a clinical trial and enhance the protection of human research participants and the informed consent process. Effective and efficient review of AEs has been a long-standing challeng...

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Published inThe journal of research administration Vol. 38; no. 1; pp. 75 - 83
Main Authors Fedor, Carol, Cola, Philip, Polites, Stephanie
Format Journal Article
LanguageEnglish
Published Washington Society of Research Administrators, Inc 22.03.2007
Society of Research Administrators
Subjects
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ISSN1539-1590
2573-7104

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Abstract The reporting, analysis, and management of adverse events (AEs) provide an ongoing assessment of risk in the context of a clinical trial and enhance the protection of human research participants and the informed consent process. Effective and efficient review of AEs has been a long-standing challenge for Institutional Review Boards (IRBs) and Research Administration programs, especially as protocols and ethical/legal issues become more complex. Furthermore, AE reporting is governed by many different regulations and sources, with inconsistencies in standards and requirements. Reporting standards for AEs were adopted when single-center clinical trials were the norm. With the increased prevalence of multi-center trials, IRBs are now inundated with AE reports. This paper will review the current issues in AE reporting and the challenges encountered by research administration programs when reassessing current policies and procedures and implementing a significantly revised reporting policy. The implementation plan and educational strategies used with the investigators and research staff will be described. Preliminary outcome data will be presented to evaluate policy revisions and to take into consideration the concepts of "quality of review" versus "quantity of reporting."
AbstractList The reporting, analysis, and management of adverse events (AEs) provide an ongoing assessment of risk in the context of a clinical trial and enhance the protection of human research participants and the informed consent process. Effective and efficient review of AEs has been a long-standing challenge for Institutional Review Boards (IRBs) and Research Administration programs, especially as protocols and ethical/legal issues become more complex. Furthermore, AE reporting is governed by many different regulations and sources, with inconsistencies in standards and requirements. Reporting standards for AEs were adopted when single-center clinical trials were the norm. With the increased prevalence of multi-center trials, IRBs are now inundated with AE reports. This paper will review the current issues in AE reporting and the challenges encountered by research administration programs when reassessing current policies and procedures and implementing a significantly revised reporting policy. The implementation plan and educational strategies used with the investigators and research staff will be described. Preliminary outcome data will be presented to evaluate policy revisions and to take into consideration the concepts of "quality of review" versus "quantity of reporting."
The reporting, analysis, and management of adverse events (AEs) provide an ongoing assessment of risk in the context of a clinical trial and enhance the protection of human research participants and the informed consent process. Effective and efficient review of AEs has been a long- standing challenge for Institutional Review Boards (IRBs) and Research Administration programs, especially as protocols and ethical/legal issues become more complex. Furthermore, AE reporting is governed by many different regulations and sources, with inconsistencies in standards and requirements. Reporting standards for AEs were adopted when single-center clinical trials were the norm. With the increased prevalence of multi-center trials, IRBs are now inundated with AE reports. This paper will review the current issues in AE reporting and the challenges encountered by research administration programs when reassessing current policies and procedures and implementing a significantly revised reporting policy. The implementation plan and educational strategies used with the investigators and research staff will be described. Preliminary outcome data will be presented to evaluate policy revisions and to take into consideration the concepts of "quality of review" versus "quantity of reporting." [PUBLICATION ABSTRACT]
Audience Academic
Author Cola, Philip
Fedor, Carol
Polites, Stephanie
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SubjectTerms Analysis
Clinical trials
Compliance (Legal)
Educational Methods
Educational Strategies
Federal regulation
Forecasts and trends
Government regulation
Human subjects
Laws, regulations and rules
Legal Problems
Market trend/market analysis
Medical research
Medicine, Experimental
Patient safety
Report writing
Reprography
Research Administration
Review boards
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Title The role of a research administration program in adverse event reporting
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