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  • Webinars
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Webinar: Protecting Human Subjects in Qualitative Research: Ethical Considerations for IRBs and Researchers

The goal of this webinar was to provide IRB members with a better understanding of the issues that qualitative researchers face and to introduce strategies to address...

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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.

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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

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Webinar: Archive (Pre-2015 Included)

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Webinar: (2022-06) Are We Excluding Pregnant People too much from Research? Ethical and Pragmatic Consequences and a Responsible Way Forward

Widespread exclusion of pregnant people from clinical research has resulted in significant evidence gaps for this population, despite an urgent need for...

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Webinar: (2022-05) Un-Common Rules: Navigating FDA-Regulated Research and the IRB

IRB review of FDA-regulated research requires the interpretation and application of regulatory standards that are different from and often in addition to those of the...

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Webinar: (2022-05) Complex Conflict of Interest (COI): Understanding the COI Landscape

This session will help the research community understand conflicts and methods of conflict management so we can be better stewards of the public trust in research....

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Webinar: (2022-03) New Guidelines for Human Stem Cell-Related Research: Implications for IRBs and Institutions

There have been stunning scientific advances in human stem cell-related research that abut an array of ethical and regulatory issues. To help address these issues at a...

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Webinar: (2022-02) Nurturing a Healthy Post-Approval Monitoring (PAM) Program: A Case-Based Approach

Do you stay up at night worrying that your PAM program isn’t successful and growing the way you envisioned? During this interactive session, the speakers will present...

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Webinar: (2022-01) Health Literacy and Human Research Protections: How the IRB Can Make Research More Understandable

Patients, participants, and their caregivers should be provided with understandable research information. IRBs can play an important role in ensuring...

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Webinar: (2021-11) More Meaningful Metrics to Assess Animal Program Quality and Effectiveness: A Review and Extension

In this session, a review (the rebroadcast of select clips from IACUC21) and extension of the popular session, the speakers will offer concrete examples of the...

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Webinar: (2021-10) Navigating the Intersections Between Animal Care and Use and Human Subjects Oversight: Mind the Gap

This session will address the intersection (and gaps!) between IACUC and IRB oversight, and will provide examples to illustrate ways these intersections and gaps can...

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Webinar: (2021-09) LGBTQIA+ Equity in Human Subjects Research: Strategies for Justice-Focused IRBs

In this webinar, the presenters will discuss LGBTQIA+ health disparities, explore inclusive research data collection methods, and introduce meaningful strategies for...

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Webinar: (2021-08) IRB Review of Expanded Access Protocols that Collect Real World Data: Considerations and Guidance

In this webinar, we will discuss key ethical and regulatory considerations and best practices for IRBs when reviewing EA protocols, both for single patients and...

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