PRIMR24 Full Schedule
Thank you for attending PRIMR24! You have 90 days to access the session recordings and evaluations, which will be unavailable after February 28, 2025. PRIM&R members will have free access to the recordings starting November 17, 2026, one year after the conference. Contact registration@primr.org with questions.
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- PRIMR24 Full Schedule
- Wednesday, November 20, 2024
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7:00 AM – 7:45 AM PT
PRIMR24 Morning Beverage Service
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7:00 AM – 7:45 AM PT
PRIMR24 Morning Beverage ServiceLocation: Flex Hall BC
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7:00 AM – 12:00 PM PT
Registration Open
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7:00 AM – 12:00 PM PT
Registration OpenLocation: Flex Hall B
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7:00 AM – 8:15 AM PT
Federal Agency, Accrediting Body, CIP/CPIA Council Office Hours
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7:00 AM – 8:15 AM PT
Federal Agency, Accrediting Body, CIP/CPIA Council Office Hours -
7:30 AM – 8:30 AM PT
Opening General Session: More Cure, Less Side Effects: A Potential Role for Preclinical Studies
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7:30 AM – 8:30 AM PT
Opening General Session: More Cure, Less Side Effects: A Potential Role for Preclinical StudiesLocation: Ballroom 1
Moderator: – Novartis Institutes for Biomedical Research
Panelist: – Novartis Biomedical Research
Panelist: – Digital In Vivo Alliance
Emerging Research Challenges and Breaking IssuesIACUC ReviewIRB ReviewPharma/Biotech Perspectives
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8:45 AM – 10:00 AM PT
PRIMR24 Plenary/Breakout/Networking G Series
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8:45 AM – 10:00 AM PT
G01 - Are the Ways We Contemplate Risk Outdated?Location: Ballroom 2
Speaker: – National Institutes of Health
Speaker: – Sage Bionetworks
Speaker: – National Human Genome Research Institute, National Institutes of Health
Emerging Research Challenges and Breaking IssuesIRB ReviewHRPP/IRB Management and Administration
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8:45 AM – 10:00 AM PT
G02 - Change the Game By Working Together: Tips for Increasing HRPP/IRB and Researcher CollaborationLocation: Ballroom 1
Speaker: – The Pennsylvania State University
Speaker: – Institute of Health System Science, Feinstein Institutes for Medical Research, Northwell Health
IRB ReviewHRPP/IRB Management and AdministrationSocial, Behavioral, and Educational Research
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8:45 AM – 10:00 AM PT
G03 - A Dialogue with OHRPLocation: Room 431-432
Speaker: – Office for Human Research Protections
Speaker: – DHHS Office for Human Research Protections
Speaker: – DHHS, Office for Human Research Protections (OHRP)
Speaker: – HHS OFFICE FOR HUMAN RESEARCH PROTECTIONS
Speaker: – Department of Health and Human Services
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8:45 AM – 10:00 AM PT
G04 - Expectations for the Use of Electronic Systems to Conduct Clinical Trial Activities and Considerations for IRBs: Perspectives From Regulators and Institutional Review BoardsLocation: Room 343-344
Speaker: – Clemson University
Speaker: – CDER/FDA/OC/OSI/DCCE
Speaker: – FDA/CDER/OC/OSI/DCCE
FDA Regulated ResearchHRPP/IRB Management and AdministrationPharma/Biotech PerspectivesQA/QI and Postapproval Monitoring
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8:45 AM – 10:00 AM PT
G05 - Reserved for Late-Breaking -
8:45 AM – 10:00 AM PT
G06 - Managing Dual/Multiple Relationships: Grappling With Identity and Interpersonal Boundaries in Human Subjects ResearchLocation: Room 445-446
Speaker: – Mass General Brigham
Speaker: – The Fenway Institute
Emerging Research Challenges and Breaking IssuesHRPP/IRB Management and AdministrationAdvancing Equity and Justice
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8:45 AM – 10:00 AM PT
G07 - Exploring the Enigma of the Expedited (Category 7)Location: Ballroom 3
Speaker: – Indiana University
Speaker: – University of California San Francisco
Social, Behavioral, and Educational ResearchIRB Review
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8:45 AM – 10:00 AM PT
G08 - Let It Go! Strategies to Prevent Over-Regulation During Local Context ReviewLocation: Signature Room
Speaker: – The Pennsylvania State University
Speaker: – University of Minnesota
Speaker: – Research Compliance Services, University of Nebraska - Lincoln
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8:45 AM – 10:00 AM PT
G09 - IBC and IRB Collaboration: Working Together for Safety and OversightLocation: Room 331
Speaker: – Advarra
Speaker: – University of Washington
Speaker: – Seattle Children's Research Institute
Shared Research Oversight ChallengesHRPP/IRB Management and Administration
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8:45 AM – 10:00 AM PT
G10 - PLENARY: Replicability, Reproducibility, Rigor, and Red HerringsLocation: Room 320-321
Moderator: – Coridea, LLC
Panelist: – Texas A&M University System
Panelist: – University of Florida College of Medicine
Emerging Research Challenges and Breaking IssuesAnimal Well-Being and the 3RsIACUC Review
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8:45 AM – 10:00 AM PT
G11 - Agricultural Animals in ResearchLocation: Room 323-324
Speaker: – Oklahoma State University
Speaker: – Veterans Health Administration, Office of Research Oversight, The Research Safety and Animal Welfare Team
Oversight of Non-Typical Animals and SituationsIACUC ReviewIACUC Fundamentals
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8:45 AM – 10:00 AM PT
G12 - Better Together-Effective Collaboration During IACUC Protocol ReviewLocation: Room 347-348
Speaker: – Arizona State University
Speaker: – Novartis Biomedical Research, Inc.
Speaker: – Texas A&M University System
IACUC ReviewACU/IACUC Program Management and Administration
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8:45 AM – 10:00 AM PT
G13 - PLENARY: Ethical Review of Human and Animal Subjects Research ProposalsLocation: Room 423-425
Moderator: – Novartis Institutes for Biomedical Research
Panelist: – Landi Animal Research and Bioethics
Panelist: – The Johns Hopkins University
Panelist: – University of North Carolina at Chapel Hill
Shared Research Oversight ChallengesResearch Oversight Leaders and Institutional OfficialsIRB ReviewIACUC Review
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8:45 AM – 10:00 AM PT
G14 - No Findings? No Problem: Why Non-Issue Audits Still MatterLocation: Room 333-334
Speaker: – Penn State
Speaker: – Indiana University
Speaker: – Harvard T.H. Chan School of Public Health
IRB FundamentalsIACUC FundamentalsQA/QI and Postapproval Monitoring
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8:45 AM – 10:00 AM PT
G15 - Building Bridges: Towards an International Framework for Specimen Sharing (Part II)Location: Room 335
Speaker: – BIopreservation & Biobanking
Speaker: – Takeda
Speaker: – Center for Integrative Medical Sciences, RIKEN
Speaker: – ARC-Net and Department of Engineering for Innovative Medicine, University of Verona, Italy
Pharma/Biotech PerspectivesResearch Involving Data and New TechnologiesIRB Review
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10:00 AM – 10:30 AM PT
Break in the Exhibit Hall
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10:00 AM – 10:30 AM PT
Beverage Break in the Exhibit HallLocation: Flex Hall BC
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10:30 AM – 11:45 AM PT
PRIMR24 Plenary/Breakout/Networking H Series
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10:30 AM – 11:45 AM PT
H01 - PLENARY: Regulatory and IRB Challenges in Reviewing Decentralized Clinical Trials (DCTs)Location: Room 323-324
Moderator: – Department of Veterans Affairs
Panelist: – DHHS Office for Human Research Protections
Panelist: – Decentralized Trials and Research Alliance
Panelist: – NCATS/NIH
FDA Regulated ResearchHRPP/IRB Management and AdministrationIRB Review
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10:30 AM – 11:45 AM PT
H02 - Group Harm: A Toolkit for Researchers, IRBs, and Data Access CommitteesLocation: Ballroom 2
Speaker: – Maimonides Medical Center
Speaker: – Johns Hopkins Bloomberg School of Public Health
Speaker: – University of Washington School of Medicine
Populations Requiring Additional ProtectionsIRB ReviewSocial, Behavioral, and Educational Research
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10:30 AM – 11:45 AM PT
H03 - Houston, We Have Problem: Exploring Noncompliance in a Single IRB (sIRB) UniverseLocation: Ballroom 3
Speaker: – Baptist Health South Florida
Speaker: – University of Texas, MD Anderson Cancer Center
Speaker: – BRANY IRB
Single IRBQA/QI and Postapproval Monitoring
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10:30 AM – 11:45 AM PT
H04 - Comparative Effectiveness Research (CER): When Important Research Does Not Fit the Regulatory MoldLocation: Room 431-432
Speaker: – Advarra
Speaker: – National Institutes of Health
Speaker: – WCG
Speaker: – None
IRB ReviewEmerging Research Challenges and Breaking Issues
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10:30 AM – 11:45 AM PT
H05 - Pharma Perspectives on the Use of Social Media and Social Media Influencers in Clinical ResearchLocation: Room 335
Speaker: – Takeda Pharmaceuticals
Speaker: – Johnson & Johnson
Speaker: – WCG
Pharma/Biotech PerspectivesEmerging Research Challenges and Breaking Issues
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10:30 AM – 11:45 AM PT
H06 - What Are You Going To Do With My Specimens and Data? When Research Specimens and Data are Used for Commercial ProfitLocation: Signature Room
Speaker: – Huron Consulting Group
Speaker: – BIopreservation & Biobanking
Speaker: – Takeda
Speaker: – ARC-Net and Department of Engineering for Innovative Medicine, University of Verona, Italy
Research Involving Data and New TechnologiesLegal Considerations in Research OversightIRB ReviewPharma/Biotech Perspectives
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10:30 AM – 11:45 AM PT
H07 - PLENARY: Protecting Third Parties in Research: Whose Job Is it Anyway?Location: Room 347-348
Moderator: – Multi-Regional Clinical Trials Center of Brigham and Women's Hospital and Harvard
Speaker: – Virginia Tech
Speaker: – Sabai - www.sabaiglobal.com
Shared Research Oversight Challenges
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10:30 AM – 11:45 AM PT
H08 - A Dialogue With the Environmental Protection Agency (EPA)Location: Room 331
Speaker: – U.S. EPA
Speaker: – Oak Ridge Associated Universities
Speaker: – US EPA
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10:30 AM – 11:45 AM PT
H09 - Exempt Study Review: How to Find Flexibilities in the Current RegulationsLocation: Ballroom 1
Speaker: – UC San Diego
Speaker: – University of California, Irvine, IRB
Speaker: – Office for Human Research Protections (OHRP), Department of Health and Human Services (HHS)
IRB ReviewSocial, Behavioral, and Educational ResearchIRB Fundamentals
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10:30 AM – 11:45 AM PT
H10 - Making the 3Rs More Than a Checkbox: Institutional 3Rs ProgramsLocation: Room 333-334
Speaker: – University of Washington
Speaker: – Eli Lilly and Company
Speaker:
Animal Well-Being and the 3RsIACUC ReviewACU/IACUC Program Management and Administration
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10:30 AM – 11:45 AM PT
H11 - Oversight of Animal Care and Veterinary Staff Qualifications and TrainingLocation: Room 320-321
Speaker: – University of Pennsylvania
Speaker: – University of Washington
Speaker: – Oregon National Primate Research Center, Oregon Health & Science University
Education, Qualifications, and TrainingIACUC Fundamentals
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10:30 AM – 11:45 AM PT
H12 - Adverse Events and Animal Welfare in Biotech and Academia Alike: Creating Efficiency, an Open Program, and Automated Functions of ReportingLocation: Room 345-346
Speaker: – UC Berkeley
Speaker: – Novartis Biomedical Research, Inc.
Pharma/Biotech PerspectivesQA/QI and Postapproval MonitoringIACUC ReviewACU/IACUC Program Management and Administration
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10:30 AM – 11:45 AM PT
H13 - Tick-Tock! How to Not Waste Your Time While Writing Minutes!Location: Room 423-425
Speaker: – Independent Professional
Speaker: – Office for Human Research Protections (OHRP)
Speaker: – Office of the Chief Medical Officer, FDA
FDA Regulated ResearchIRB ReviewIRB FundamentalsIACUC FundamentalsIACUC Review
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10:30 AM – 11:45 AM PT
H14 - Don't Reinvent the Wheel! How to Ask the Right Questions and Leverage Existing Resources to Address Critical Compliance NeedsLocation: Room 445-446
Speaker: – University of Nevada, Las Vegas
Speaker: – Western Washington University
Speaker: – KBR
Education, Qualifications, and TrainingShared Research Oversight ChallengesHRPP/IRB Management and AdministrationACU/IACUC Program Management and AdministrationQA/QI and Postapproval Monitoring
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10:30 AM – 11:45 AM PT
H15 - Considering Yourself: SelfâCare for Compliance ProfessionalsLocation: Room 343-344
Speaker: – University of Texas at Arlington
Speaker: – Lawrence Berkeley National Laboratory
Education, Qualifications, and TrainingShared Research Oversight ChallengesHRPP/IRB Management and AdministrationACU/IACUC Program Management and Administration
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12:00 PM – 5:00 PM PT
Bridging the Gap: Showcasing the University of Washington (UW) Animal Research Facilities and Program
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12:00 PM – 5:00 PM PT
Bridging the Gap: Showcasing the University of Washington (UW) Animal Research Facilities and Program
