The Microbicide Trials Network: Coordinating HIV Prevention Trials in Sub-Saharan Africa
Presenter(s): Sharon Hillier
Status: Available
Air Date: 9/15/2009
Air Time: 12:00 PM EST
Length: 1 Hour 3 Seconds
The Microbicide Trials Network: Coordinating HIV Prevention Trials in Sub-Saharan Africa presented by Sharon Hillier, PhD University of Pittsburgh School of Medicine, Department of Obstetrics, Gynecology and Reproductive Sciences, Magee-Womens Research Institute

Financial Conflicts of Interest: Why Should you Care? and How the University Addresses COIs
Presenter(s): Jerome L. Rosenberg, David L. Wehrle
Status: Available
Air Date: 3/17/2009
Air Time: 12:00 PM EST
Length: 44 Minutes 2 Seconds
Financial Conflicts of Interest: Why Should you Care? presented by Jerome L. Rosenberg, PhD (Chair/COI Committee & Research Integrity Officer) and
How the University Addresses COIs presented by David L. Wehrle, CPA, CIA, CFE (Director/COI Office)

Data and Safety Monitoring Plans and Data and Safety Monitoring Boards
Presenter(s): Jane Alexander, Jeannie Barone, CIP, Laurel Yasko RN, BSN, CCRC
Status: Available
Air Date: 2/17/2009
Air Time: 12:00 PM EST
Length: 51 Minutes 50 Seconds
Data and Safety Monitoring Plans and Data and Safety Monitoring Boards presented by Jane Alexander, Research Participant Advocate, Clinical and Translational Science Institute, Laura Yasko, Co-director, Regulatory Knowledge and Support Core, Clinica and Translational Science Instituteand Jeannie Barone, IRB Assistant Director

Infrastructure Resources of the CTSI – what are they and how can I access them for my research protocol?
Presenter(s): Daniel J. Buysse; M.D., Dawn Guzik Stocker
Status: Available
Air Date: 1/15/2009
Air Time: 12:00 PM EST
Length: 1 Hour 3 Minutes 54 Seconds
Infrastructure Resources of the CTSI – what are they and how can I access them for my research protocol? presented by Daniel J. Buysse, MD, Director, Participant and Clinical Interactions Resources (PCIR) Core and Director, Neuroscience CTRC and Dawn Guzik Stocker, MPA, Interim PCIR Core Administrator, N-CTRC Administrator, Braddock CTRC Administrator

Human Stem Cell Research at the University of Pittsburgh
Presenter(s): William Allen Hogge, M.D., Kyle Orwig, Ph.D., Alan Meisel, J.D., Kim Hollabaugh, MSN, RN, Richard S. Guido, MD
Status: Available
Air Date: 10/15/2008
Air Time: 12:00 PM EST
Length: 1 Hour 13 Minutes 39 Seconds
Introduction by Richard Guido
Human Stem Cell Research at the University of Pittsburgh presented by Kyle Orwig, Ph.D., Assistant Professor Department of Ob/Gyn & Reproductive Sciences
Second presenter Alan Meisel, J.D., Dickie, McCartney, and Chilcote Professor of Bioethics and Professor of Law Director, Center for Bioethics & Health Law
Third presenter W. Allen Hogge, M.D., Milton Lawrence McCall Professor and Chair Department of Ob/Gyn & Reproductive Sciences Chairman, hSCRO Committee
Fourth presenter Kim Hollabaugh, MSN, RN, Director, hSCRO Office, University of Pittsburgh

Introduction to the Office for Investigator-Sponsored IND and IDE Support (O3IS)
Presenter(s): Dennis Swanson, MS
Status: Available
Air Date: 6/12/2008
Air Time: 12:00 PM EST
Length: 1 Hour 21 Minutes 59 Seconds
Introduction to the Office for Investigator-Sponsored IND and IDE Support (O3IS) presented by Dennis P. Swanson, MS, Professor and Assistant Dean School of Pharmacy, Director, Office for Investigator-Sponsered IND and IDE Support, University of Pittsburgh

Highlights of Good Research Practice
Presenter(s): Nancy Nagel, RN, BSN, CCRC, Patricia Erb, RN, BSN, Cynthia Kern, RN, CIP, Kim Hollabaugh, MSN, RN
Status: Available
Air Date: 5/15/2008
Air Time: 1:00 PM EST
Length: 1 Hour 2 Minutes 21 Seconds
Staff of the Education and Compliance Office presents Highlights of Good Research Practice
"Welcome and Introduction" by Nancy Nagel, RN, BSN, CCRC
"Protocol Adherence & Oversight" by Patricia Erb, RN, BSN
"Informed Consent" by Nancy Nagel, RN, BSN, CCRC
"Study Documentation" by Cynthia Kern, RN, CIP
“Drug/ Device Accountability" Kim Hollabaugh, MSN, RN

This presentation will discuss the processes involved in implementing and documenting the various activities associated with a research protocol. The presentation will serve as a review of the steps involved in preparation to conduct a research protocol. A review of the proper methods to conduct and document the informed consent process will be included as well a summary of the required documentation and supportive source documents that should be maintained as a matter of Good Research Practice.

Tissue Banks:Legal Considerations and Compensation for Injury
Presenter(s): Theresa Colecchia, Esq., Alex Ciocca, Esq.
Status: Available
Air Date: 4/15/2008
Air Time: 12:00 PM EST
Length: 1 Hour 9 Minutes 15 Seconds
UPMC and University of Pittsburgh Legal Perspectives Related to “Tissue Banks: Legal Considerations and Compensation for Injury
presented by Theresa Colecchia, Esq. Associate General Counsel, University of Pittsburgh and Alex Ciocca, Esq. Legal Counsel, UPMC
Theresa Colecchia, Esq. Legal Counsel, University of Pittsburgh
Alex Ciocca, Esq. Legal Counsel, UPMC

Research Study Participant Payment System We-Pay
Presenter(s): Susan M. Gilbert, George J. Cerminara
Status: Available
Air Date: 3/10/2008
Air Time: 1:00 PM EST
Length: 1 Hour 3 Minutes 24 Seconds
UPMC and The University of Pittsburgh Office of Finance presents Research Study Participant Payment System "We-Pay" presented by
Susan M. Gilbert, Assistant Treasurer of Finance, University of Pittsburgh
George Cerminara, Project Consultant

Reporting of Unanticipated Problems and Adverse Events
Presenter(s): Jamie Zelazny, MPH, RN, Jeannie Barone, CIP
Status: Available
Air Date: 2/13/2008
Air Time: 12:00 PM EST
Length: 34 Minutes 21 Seconds
Reporting of Unanticipated Problems and Adverse Events
First presenter Jamie Zelazny, MPH, RN, Adverse Events Coordinator, University of Pittsburgh
Second presenter Jean Barone, CIP, Assistant IRB Director, University of Pittsburgh