Webinar: Focus on the Revised Common Rule: Informed Consent
This webinar will discuss new elements of the Rule impacting informed consent.
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Webinar: Focus on the Revised Common Rule: Exemption Categories and Select Types of Review
This webinar will examine and discuss key operational and administrative provisions in the new Rule.
Webinar: Focus on the Revised Common Rule: Biospecimens and Identifiable Private Information
This webinar will discuss provisions specific to research with biospecimens and identifiable private information under the new Rule
Webinar: Archive (Pre-2015 Included)
Webinar: (2021-07) Thorny Questions in Everyday IRB Deliberations: An Interactive, Case-Based Approach
IRB review of human subjects research consistently presents a range of ethical and regulatory challenges in even the simplest of research protocols. In this session,...
Webinar: (2021-05) Leading Up, Down, and Across Your Organization
This session will introduce leadership strategies that are effective regardless of the role you fill in your organization, and discuss best practices for implementing...
Webinar: (2021-04) Now Is No Time to Relax: Why the Global Pandemic Strengthens the Case for Considering Sex as a Biological Variable
Established five years ago in January 2016, the NIH policy on the Consideration of Sex as a Biological Variable (SABV) is a part of a global movement to integrate the...
Webinar: (2021-03) Omnium-Gatherum: An SBER Variety Show
Due to the diverse methodologies, interdisciplinary nature, and broad implications of social, behavioral, and educational research (SBER), IRBs who review SBER are...
Webinar: (2021-02) The Colors of COVID-19: Embracing the Novel Ethical Challenges and Opportunities in COVID-19 Vaccine Trials
Stephen B. Thomas, PhD, and Sandra Crouse Quinn, PhD, will present a discussion of challenges, advances, and progress regarding barriers to the involvement of...
Webinar: (2020-11) The IRB's Role in Achieving Diversity in Research
The lack of appropriate representation in subject populations is a long-standing challenge for clinical research. The IRB plays a central role in considering and...
Webinar: (2020-10) IRB Operations During a Pandemic
The SARS-CoV-2 pandemic continues to impact the entire global research enterprise. All aspects of human subjects research protections programs are seeing challenges to...
Webinar: (2020-09) IACUC Operations: Pandemic & Beyond
During the COVID-19 pandemic, IACUCs across the nation have had to adjust their operations to accommodate working remotely. This has necessitated the leveraging of...
Webinar: (2020-07) Quality Management Systems: Tools to Consider in an Animal Care and Use Program
This webinar will cover concepts, tools, and processes commonly used in a Quality Assurance (QA) or Quality Control (QC) program that can be adapted with a similarly...
Webinar: (2020-06) Complexity in Clinical Trial Design: A Primer on Adaptive and Platform Trials
During this webinar, speakers will define key terms, explore ethical and regulatory challenges, and provide strategies and examples to bridge the gap between IRBs and...
Webinar: (2020-04) Meaningful Metrics: How HRPPs Can Use Their Data Effectively
HRPPs generate an abundance of performance data and metrics. When used effectively, this information can help HRPPs meet programmatic and institutional goals, and...