|
Member Content. While some content is available to all, some is available only to PRIM&R members. Learn about this and other benefits of PRIM&R membership here. Free member content here View Product Bundles in the top toolbar.
|
Sort content in the "Browse..." pull-down menu below.
|
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...
Webinar: Focus on the Revised Common Rule: Informed Consent
This webinar will discuss new elements of the Rule impacting informed consent.
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: (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...
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...
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...
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...
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...
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...
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...
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...
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...