Webinar Follow-Up: IRB Review of Expanded Access Protocols that Collect Real World Data
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Search results for 'data'
Webinar: Focus on the Revised Common Rule: Informed Consent
This webinar will discuss new elements of the Rule impacting informed consent.
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: (2021-09) 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: (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: (2020-04) 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...
Webinar: (2019-10) Real-World Approaches to Informed Consent under the Revised Common Rule
As the end of the first year of the revised Common Rule era approaches, it’s time for a check-in: how is the human subjects research oversight community doing so far...
Webinar: (2019-06) Expectation vs. Reality: Reporting Obligations to the IRB
Understanding which events to report to the IRB is an ongoing challenge for researchers and IRBs alike. Institutional policies and procedures vary widely, which can...
Webinar: (2019-05) Data Sharing in SBER: Balancing Transparency and Human Research Protections
During this webinar, speakers will provide knowledge and strategies for IRBs to help their institution’s social scientists approach data sharing in an ethical and...
Webinar: (2018-10) Responsible Conduct of Research: What IRBs Need to Know
During this webinar, speakers will provide IRB professionals and IRB members with foundational knowledge to help connect the dots between human subjects protections...
Webinar: (2018-05) Forward-Looking Strategies for IRBs in the Genomic Age: Preparing for Shifting Concepts of Identifiability
As genetic sequencing and testing become increasingly accessible and prevalent, so too has the ability to share vast amounts of genomic information. Such advances have...
Webinar: (2018-04) EU General Data Protection Regulations: What US Research Institutions Need to Know
This webinar will provide an introduction to the potential application of the GDPR to the US-based research community; implications for individuals and institutions to...
Webinar: (2018-02) Digital Health Technology and Human Subjects Research: What IRBs Need to Know
Advances in digital health applications, tools, and technologies are occurring rapidly and are here to stay. Often, these technologies are designed to be “disruptive”...