PHRP Online Training

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PHRP Online Training

Protecting Human Research Participants Online Training (PHRP) is intended for those involved in research with human subjects.

Learn more at www.PHRPTraining.com. PHRP Online Training provides certificate training for those involved in the conduct or oversight of research involving human subjects. PHRP offers up-to-date training on human subjects protections for all involved in this research. PHRP includes:

- An engaging & interactive format with realistic case studies and exercises
- Progress tracked on a personal dashboard
- Certificates of completion always available with login
- Option to earn professional continuing education credits
- Course offered in English, Spanish, or French at no additional charge

Institutional subscriptions include:
- Complimentary on-boarding and support provided for all group administrators
- Flexible plans and centralized billing
- An institution-specific registration link
- An administrative dashboard for monitoring users and managing certificates

Visit https://phrptraining.com/ to learn more or contact us at info@phrptraining.com to schedule a demo or receive a quote on an institutional subscription.

05/11/2025

How can institutions make multi-site IRB review faster, clearer, and more consistent? PHRP Advisory Board Member Joe Smith breaks it down in his new article, "Making Reliance Work: Practical Ways to Streamline Multi-Site IRB Review." He also shares practical tools and lessons learned in the companion PHRP Perspectives podcast episode—offering a roadmap for efficient, participant-centered collaboration. Explore both resources to strengthen your institution’s reliance process. https://bit.ly/3Ji92s4

30/10/2025

Are you responsible for Human Subjects Protection training and certification at your organization? Kristen Michaelson is here to help. As PHRP’s Educational Sales Consultant, Kristen partners with institutions to tailor programs, streamline administration, and expand access to PHRP Online Training. Read more. https://bit.ly/4qAWGfh

23/10/2025

Before you collect data, ask: Is this really human subjects research?

PHRP Advisory Board Member Kim Diaccinni shares practical insights on making clear, defensible determinations—covering common pitfalls, anonymous vs. de-identified data, and how to avoid retroactive IRB approval challenges.

Her article complements the latest PHRP Perspectives podcast episode featuring Christine Wallace of Brown University.

Explore both the article and podcast here: http://bit.ly/47EfZN9

14/10/2025

How can IRBs ensure informed consent remains ethical and robust in expanded access (compassionate use) programs?

In his new article and companion PHRP Perspectives podcast, PHRP Advisory Board Member Richard Klein explores the IRB’s vital role in protecting patients and maintaining ethical standards in non-research treatment settings. https://bit.ly/4nLXcFl

02/10/2025

Universities. Hospitals. Research Centers. Corporations.
If your team works with human research participants, PHRP gives you the tools to stay compliant and efficient—at scale. Request a quote today. https://bit.ly/4mDzbPs

01/10/2025

What actually speeds up multi-site approvals? On this episode of PHRP Perspectives, PHRP Advisory Board Member Joe Smith and Vidhi Rami from the University of Maryland share what works: clear roles, organized trackers, consistent check-ins, and lightweight researcher intake. They also cover when reliance isn’t appropriate and why some institutions decline. Listen for a concise, real-world guide for IRB/HRPP teams and investigators. http://bit.ly/3IL3k1r

30/09/2025

Reliance agreements and single-IRB review can dramatically reduce duplicate work in multi-site research. In our new PHRP Perspectives episode, Joe Smith and Vidhi Rami will explain how reviewing vs. relying institutions share responsibilities, where local context fits, and the practical steps to keep collaborations on track. Catch the episode tomorrow.

25/09/2025

Is your research team fully trained in human subjects protection?
PHRP Online Training delivers accredited, Common Rule-aligned training built for institutions. Scalable plans. Trusted by 500+ organizations. Book a demo today. 👉 https://bit.ly/4mDzbPs

22/09/2025

Community outreach is more than a checkbox—it’s the foundation of trust between IRBs, researchers, and the public. PHRP Advisory Board Member Joe Smith explores this topic in his article, "Building Better Bridges: Improving IRB Community Outreach," highlighting strategies that include building partnerships, listening to feedback, and tailoring approaches to unique institutional settings.

The companion PHRP Perspectives podcast episode with Joe and guest expert Samantha Martocci dives deeper into practical ways IRBs can connect meaningfully with the communities they serve.

Explore the article and podcast: https://bit.ly/3KfyEpl

08/09/2025

Clear and consistent non-human subjects determinations protect institutions and help researchers stay on track. In this PHRP Perspectives episode, PHRP Online Training Advisory Board Member Kim Diccianni and her guest, Christine Wallace, explain how institutions can strengthen policies, streamline decision-making, and improve trust between and investigators. Kim provides a preview of the full episode. https://bit.ly/42dUD69

03/09/2025

When does research fall outside the scope of IRB oversight? In this episode of PHRP Perspectives, PHRP Online Training Advisory Board Member Kim Diccianni and Christine Wallace, regulatory advisor at Brown University, discuss how institutions make non-human subjects determinations. They share best practices for clear communication, documentation, and collaboration to ensure researchers and IRBs are aligned.

Listen or watch here: https://bit.ly/42dUD69

13/08/2025

How can support ethical decision-making when investigational drugs are used outside of clinical trials? In this episode of PHRP Perspectives, longtime FDA and HHS leader Richard Klein and NYU medical ethics expert Lisa Kearns explore the role of IRBs in treatment use, the differences between expanded access and Right to Try, and how informed consent protects patient rights.🎧 Listen to the full episode: https://bit.ly/40Nl1Dl

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https://www.phrptraining.com/

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