Presentation Library

Overview of Institutional Review Board Requirements (pps)

Informed Consent of Non-English Speaking Research Subjects (PPS)

Standards for Approval Pending Minor Revisions - IRB Member Module (pps)

Risk Assessment - IRB Member Module (PPS)

Compensation for Research Participation - IRB Member Module (PPS)

Research with "Secondary" or "Third Party Subjects" - IRB Member Module (PPS)

Completing IRB Submission Materials: Part 1- Description of Study (How to Navigate the IRB Process) (PPS)

The following presentations were presented at the National Research Forum, entitled "Thinking Outside the Box:  Addressing the Challenges of Human Subject Research in 2008" on February 8, 2008 in Sacramento:

Keynote: “Preparing Ahead for Disaster and Traumatic Stress Research” – Roxane Cohen Silver, PhD (PPS)

Plenary Presentation – Gigi McMillan, BA (PPS)

“What’s New from the Feds? OHRP Update” – Ivor Pritchard, PhD (PPS)

“What’s New in the Department of Defense?” – Patty Decot (PPS)

“Alternative Models of IRB Review” – Sarah Fowler-Dixon, PhD (PPS)

“Alternative Models of IRB Review” - Tony Perez, JD (PPS)

“California Information Security and Privacy Protection Requirements and Changes in the Information Practices Act (SB 13) – Larry Dickey, MD, MPH, MSW (PPS)

“California Information Security and Privacy Protection Requirements” Colleen Pedroza, BA (PPS)

“Clarifying the Role of IRB Members & Administrative Staff: Regulatory Requirements & Responsibilities” - Kevin L. Nellis, MS, MT (ASCP) (PPS)

“Data Security and Universities” – Rory Jaffe, MD, MBA (PPS)

“Education of Researchers” – Sarah Fowler-Dixon, PhD (PPS)

“Education of Researchers” – Lisa M. Voss, MPH, CIP (PPS)

“FDA Perspective on “Adverse Events” – Sara F. Goldkind, MD, MA (PPS)

“Human Subject Protections: Regulations and Guidance” – Lyndi Lahl, MS, RN and Kevin Nellis, MS, MT (ASCP) (PPS)

“IRB Staff: Roles and Responsibilities” - Helen McGough, MA, CIP (PPS)

“IRB Review in CTSA Sites” – Sara Fowler-Dixon, PhD and Tony Perez, JD (PPS)

“Nuts and Bolts of IRBs” – George Gasparis (PPS)

“Protection of Research Participants: CIRM’s Comprehensive Approach” – Geoffrey Lomax, Dr. PH (PPS)

“Reviewing and Reporting Adverse Events/Unanticipated Problems: FDA & OHRP Guidance” – Lyndi Lahl, MS, RN (PPS)

“Role of IRB Members & Staff” - David Asmuth, MD (PPS)

“Should IRBs Review Program Evaluation Activities?” – Helen McGough, MD, CIP (PPS)

“Stem Cell Research: ESCRO Committees, IRBs, and Ethics” – Michael Kalichman, PhD (PPS)

“Student Research and Student Researchers: 2 (of many) issues” – Helen McGough, MA, CIP (PPS)

“Student Research – Two Perspectives” – Ed Nelson, PhD (PPS)

“Student Research and Institutional Review Boards” – Carrie Saetermoe, PhD (PPS)

“University of Michigan Demonstrations and Innovations in Non-federally Funded Research” – Judith Birk, JD and Pam Smock, PhD (PPS)