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Newsletter


Keep up with us!  

2013 Winter-1

The HRPP Newsletter is a great source of information regarding new developments within the HRPO. These will be circulated twice yearly.


Archive

Winter 2013

Summer 2013

Winter 2012

Summer 2012

Winter 2011

Summer 2011

Winter 2010

Summer 2010

Winter 2009

Summer 2009

Education and Training

Please see the Seminars and Workshops that the Tulane HRPO has presented to the Research Community below.



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  

03/21/2013

Clinical Coordinator Informational Session

01/18/2013

Social/Behavioral IRB Member Informational Session

09/07/2012

Social/Behavioral IRB Research Workshop

05/11/2012

Investigator Responsibilities in Human Subjects Research

04/12/2012

Ensuring Patient Safety and Scientific Quality

03/20/2012

Social/Behavioral IRB Research Workshop

02/09/2012

The Ten Most Common Mistakes in IRB Submissions

12/01/2011

Research Coordinator "Ask the IRB" Session

10/25/2011

Navigating the IRB

07/07/2011

New Investigator and Student Research Training

04/26/2011

IRB Consideration and Review of Data and Safety Monitoring Plans

03/02/2011

Workshop for Social/Behavioral Research - 10 Steps to IRB Approval, HRPO Web Site, IRBNet, and International Research

11/29/2010

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

10/19/2010 10/21/2010

Navigating the HRPP web site, IRBNet, and IRB Submissions

08/03/2010

Scientific Review, ICH-GCP, Unanticipated Problems, and Possible IRB Actions

05/06/2010

Required Findings and Determinations presented by Jeffrey Cohen, HRP Associates, Inc.

04/27/2010

HRPO SOPs and ICH-GCP

03/02/2010

Workshop for Social/Behavioral Research

03/01/2010

Oral Histories and Human Subjects Research Protection Requirements 

12/14/2009

IRB Meetings, Preparing Responses to IRB Decisions and Issues with IRBNet

10/12/2009 - 10/16/2009

IRBNet Training Sessions

09/29/2009

Reporting Unanticipated Problems and Protocol Deviations and Violations

Checklists, Auditing, and Reporting Unanticipated Problems and Protocol Deviations and Violations

09/01/2009

Tulane University Accreditation with AAHRPP

06/23/2009

The Informed Consent Process

05/12/2009

Ethics in Global Health Research Seminar

02/16/2009

Checklists, Federal Regulations, Continuing Reviews, Unanticipated Problems and Protocol Deviations

06/04/2008

Compliance: Protecting Subjects and Protecting Research

11/15/2007

Human Research Submission and Review Process - Biomedical

11/06/2007

Human Research Submission and Review Process - Social/Behavioral



 

Institutional Review Board, New Orleans, LA 70112 504-988-2665 irbmain@tulane.edu