PHRP Perspectives is your go-to resource for navigating ethics, compliance, and best practices in human subjects research. Each episode delivers expert insights, practical advice, and real-world stories to help you stay ahead and make informed decisions. PHRP Perspectives is brought to you by PHRP Online Training.
From Oversight to Impact: Advancing Quality in Human Research Programs
In this episode of PHRP Perspectives, Joe Smith talks with Andrea Dragan, Director of Quality Assurance and Evaluation at Rutgers University, about the evolving role of quality assurance in human research. They discuss how Human Research Protection Programs can balance compliance and innovation, build stronger partnerships with investigators, and use education and transparency to support ethical research and participant protections. Show Notes: Joe Smith and Andrea Dragan explain qual...
1 Oct 2025
Reliance Agreements and Collaborating with HRPPs
Join PHRP Perspectives as we explore the increasingly important world of reliance agreements in human subjects research. In this episode, Joe Smith and Vidhi Rami from the University of Maryland walk us through how these agreements reduce administrative burden, streamline IRB reviews, and ensure regulatory compliance in multi-site studies. In this episode of PHRP Perspectives, Advisory Board member Joe Smith sits down with Vidhi Rami (IRB Specialist, Reliance Agreements) to demystify reliance...
2 Sept 2025
Non-Human Subjects Determinations
If you’ve ever struggled with deciding whether your project qualifies as human subjects research, you’re not alone. Compliance veterans Kim Dicciani (PHRP Online Training Board Member) and Christine Wallace break down the definitions, edge cases, and institutional policies that shape IRB determinations—and share practical guidance every researcher can use. Show Notes: Kim Dicciani and Christine Wallace break down key definitions, intent, and misconceptions on IRB review and...
6 Aug 2025
IRB Considerations for Treatment Use Protocols in Investigational Products
What role do IRBs play when investigational drugs are used for treatment? PHRP Advisory Board Member and longtime FDA and HHS leader Richard Klein and Lisa Kearns, Senior Research Associate in the division of Medical Ethics at NYU's Grossman School of Medicine, provide clarity on the ethical and regulatory frameworks behind expanded access, Right to Try laws, and the pivotal function of informed consent. Show Notes: Richard and Lisa explore IRB considerations for compassionate us...
17 Jul 2025
Improving IRB Community Outreach Methods
How can IRBs and research investigators improve outreach within their institutions and with the broader community? Joe Smith, PHRP Advisory Board Member and Director of the Human Research Protection Program at University of Maryland College Park and Samantha Martocci, IRB Specialist in Education and Improvement with the University of Maryland, discuss how to better connect, communicate, and collaborate to build stronger internal and external engagement. Show Notes: Joe Smit...
8 Jul 2025
PHRP Perspectives - Podcast Trailer
New Podcast Launch: PHRP Perspectives: Ethics, Research & Compliance We're excited to introduce PHRP Perspectives — your new go-to podcast for ethics, compliance, and best practices in human subjects research. Featuring leading voices in the field, our first season dives into: - Informed consent and expanded access - Community outreach and IRB reliance agreements - Human subject research determinations and compliance tools Join PHRP Advisory Board Members Richard Klein, Joe Smit...
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YouTube views
6,355
Score snapshot 15 Sept 2025
Apple Podcasts (US)
5.0 / 5
1 ratings
Podcast Authority Score: 51 / 100
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Quality
73
Social presence
0
YouTube
74
Engagement
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