Listed below are all the seminars and workshops the Tulane HRPO has presented over time.
General Presentations
The Institutional Review Boards (IRBs) and Human Subjects Research Protection Programs: A Short Course
An Overview of Basic IRB Regulations
Seminars and Workshops
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03/21/2013
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Clinical Coordinator Informational Session
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01/18/2013
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Social/Behavioral IRB Member Informational Session
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05/11/2012
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Investigator Responsibilities in Human Subjects Research
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04/12/2012
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Ensuring Patient Safety and Scientific Quality
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03/20/2012
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Social/Behavioral IRB Research Workshop
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02/09/2012
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The Ten Most Common Mistakes in IRB Submissions
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12/01/2011
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Research Coordinator "Ask the IRB" Session
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10/25/2011
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Navigating the IRB
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07/07/2011
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New Investigator and Student Research Training
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04/26/2011
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IRB Consideration and Review of Data and Safety Monitoring Plans
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03/02/2011
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Workshop for Social/Behavioral Research - 10 Steps to IRB Approval, HRPO Web Site, IRBNet, and International Research
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11/29/2010
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FDA Inspections
Maintaining the Site's Regulatory Binder
Site Monitoring Reports
Identifying, Correcting, and Preventing Common Errors in Clinical Research
Presented by Aureus Research Consultants, LLC
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10/19/2010 10/21/2010
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Navigating the HRPP web site, IRBNet, and IRB Submissions
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08/03/2010
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Scientific Review, ICH-GCP, Unanticipated Problems, and Possible IRB Actions
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05/06/2010
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Required Findings and Determinations presented by Jeffrey Cohen, HRP Associates, Inc.
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04/27/2010
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HRPO SOPs and ICH-GCP
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03/02/2010
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Workshop for Social/Behavioral Research
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03/01/2010
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Oral Histories and Human Subjects Research Protection Requirements
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12/14/2009
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IRB Meetings, Preparing Responses to IRB Decisions and Issues with IRBNet
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10/12/2009 - 10/16/2009
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IRBNet Training Sessions
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09/29/2009
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Reporting Unanticipated Problems and Protocol Deviations and Violations
Checklists, Auditing, and Reporting Unanticipated Problems and Protocol Deviations and Violations
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09/01/2009
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Tulane University Accreditation with AAHRPP
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06/23/2009
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The Informed Consent Process
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05/12/2009
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Ethics in Global Health Research Seminar
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02/16/2009
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Checklists, Federal Regulations, Continuing Reviews, Unanticipated Problems and Protocol Deviations
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06/04/2008
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Compliance: Protecting Subjects and Protecting Research
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11/15/2007
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Human Research Submission and Review Process - Biomedical
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11/06/2007
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Human Research Submission and Review Process - Social/Behavioral
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