​This session will explore strategies for engaging HRPP stakeholders and discuss key compliance approaches and touchpoints over the life of a research project. Case...

Occasional instances of noncompliance or misconduct, or other research integrity violations, can occur in any research setting. Identification of the factors leading...

Despite improvements over the last two decades in the inclusion of women as participants in clinical trials, women are still underrepresented in trials for some...

​Over the last decade, advances in digital technology and the proliferation of mobile devices have afforded researchers unprecedented access to massive amounts of data...

​With so much competition for experienced research administrators, lab personnel, and animal care staff, it can be beneficial to seek IACUC staff outside of the common...

​In this session, we will provide an overview of the debate and regulatory issues in chimeric research and discuss one or two illustrative case studies that identify...

Acknowledging, respecting, and preserving the bond between research animals and their human caregivers is vitally important for the well-being of all participants in...

​During this webinar, panelists from the Consortium to Advance Effective Research Ethics Oversight (www.aereo.org) will discuss several recent empirical studies,...

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

As artificial intelligence research continues to evolve, those working in human subjects protections are faced with new and unique challenges working under the current...

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....

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...

This virtual roundtable will discuss best practices to create and foster effective communications throughout an entire IRB submission cycle. The presenter will explore...

Notable Landmarks: Other Requirements You Need to Know. ​Responsibilities beyond the IRB review process that the Common Rule outlines and that IRB administrators might...

This session is geared towards people who are coming up on their June 30 deadline to recertify, and they're recertifying by CEs for the first time. There will also be...

The Main Attraction: Regulations Related to the Review Process. Key sections of the Common Rule that relate to IRB review activities

This session is geared towards people who are coming up on their June 30 deadline to recertify, and they're recertifying by CEs for the first time. There will be Q&A...

Getting There: Discovering the Common Rule | What is the Common Rule, where can you find it, and how do you read it?

This session, which includes bioethics members of the global task force that updated the guidelines, will guide attendees through important IRB-specific aspects of the...

Originally presented at the 2021 Advancing Ethical Research Conference, sessionD02: Embedding a Racial Justice Lens into Research and IRB Review With Human...

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...

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

​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...

This virtual roundtable will present details of The University of New Mexico IRB office's collaboration with the university registrar to better understand each other's...

Join us for a live demonstration of PRIM&R’s new Animal Research Oversight Course (AROC)!

​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...

This case study-based Zoom meeting offers attendees the opportunity to interact with the speakers and other participants on screen. Through a combination of active...

Using researcher and student feedback, this roundtable will review the draft guidance issued by OHRP on the exemption at 104(d)(3) concerning benign behavioral...

This session will introduce leadership strategies that are effective regardless of the role you fill in your organization, and discuss best practices for implementing...

Several years into the single IRB landscape, questions related to management, communication between stakeholders, continuing review, etc., persist. Facilitated by...

The coronavirus pandemic has revealed critical gaps in our knowledge base, intransigent health disparities and health inequities, and runs the risk of reversing years...

​Due to the diverse methodologies, interdisciplinary nature, and broad implications of social, behavioral, and educational research (SBER), IRBs who review SBER are...