Virtual Roundtable: Broad Consent Provisions for Data Sharing and Use: Advising Researchers on Uses and Best Practices
Facilitated by Rachele Hendricks-Sturrup, DHSc, MSc, MA, Research Director of Real-World Evidence at the Duke-Margolis Center for Health Policy, this roundtable...
PRIM&R Member Newsletter 2023-08
Thought Leaders Weigh Research Implications when State Laws Restrict Abortion Access, REDCap for IACUC Programmatic Improvements, A Farewell from PRIM&R's Executive...
Research Ethics Digest: 2023-08
Welcome to Research Ethics Digest. The articles included in this month's issue offer an exploration into various areas of research ethics,including considerations in...
Virtual Roundtable: Research Electronic Data Capture (REDCap) as a Tool for IACUC Programmatic Improvements
This virtual roundtable discusses using REDCap, a free secure electronic application developed at Vanderbilt University, as a tool for IACUC programmatic improvements....
PRIMR22 B07 - The Need for Transparency as the Public and Legislators Weigh Legal Challenges to the Future of Research With Animals
Individual pharmaceutical and biotech companies, as well as cross industry organizations like the Institutional Officials Consortium and Interpharma, have taken steps...
Webinar: (09-2023) Questions in Everyday IRB Deliberations: An Interactive, Case-Based Approach
IRB review of human subjects research consistently presents a wide variety of ethical and regulatory challenges in even the simplest of research protocols. In this...
Webinar: (07-2023) Diversity, Equity, Inclusion, and Justice (DEIJ) Tools for IRBs
IRBs have always been charged with addressing issues of equity, justice, and access, but there is an increased need for IRBs and institutions to not only expand their...
Virtual Roundtable: Operational Best Practices for Multi-Site Studies
Through this virtual roundtable, members discuss the various successful strategies and pitfalls to avoid when operationalizing the management and oversight of...
PRIMR22 A19 - Is Your Institution Ready to Handle Open Record and FOIA Requests?
An institution should be ready to respond to FOIA requests and there are many aspects to consider. This session will provide an overview of open records and FOIA laws...
Webinar: (06-2023) Ongoing Study Oversight: Ensuring Protocol Compliance through Postapproval Monitoring
This webinar will address different models for providing ongoing study oversight through a postapproval monitoring program and how to use PAM visit results as part of...
PRIM&R Member Newsletter 2023-06
Research Ethics Digest: 2023-06
The articles included in this month's issue offer an exploration into various areas of research ethics, including special considerations in IACUC refresher training,...
Webinar: (05-2023) Implementing New NSF RCR Requirements: Key Considerations for Institutions
This panel will address upcoming changes to current National Science Foundation (NSF) requirements for education in the responsible conduct of research (RCR) as...
2023 CPIA Exam Information Session
This session will walk through the CPIA program, the exam application process, the changes to the 2023 CPIA exam format. Featuring an interview with a currently...
Workshop: (11-2023) Exploring FDA Regulations
This entry-level workshop is designed for those involved in the study, oversight, and regulation of drugs, biologics, and devices.
