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Blog

Navigating Local Considerations When Developing sIRB Reliance Policies

Explore key local considerations for developing single IRB policies, and learn how to navigate the challenges- including compliance, ethical standards, and institutional requirements.

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7 min. read
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White Paper

sIRB Review for Multicenter Research: A Guide for Institutions

February 15, 2024

Single IRB (sIRB) review for multicenter research is fast becoming the norm in the US. Initiative such as the NIH sIRB policy and revised Common Rule make it clear that ...

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E-Book

Trend Report: DE&I in Clinical Research: Where we are Today

How is the research community addressing recent regulatory actions urging improved diversity and representation in clinical trials?

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Webinar

What Happens When a Study Fails to Meet Its Recruitment Targets?

Explore IRB considerations for overcoming study enrollment barriers while ensuring risks to participants are appropriately minimized.

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Webinar

Best Practices for IRB Review of DCTs: Expert Perspectives

Leverage best practices for IRB review of decentralized trial elements sourced from research community experts.

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Blog

IBC vs. IRB: What’s the Difference?

Gene therapy research is full of promise, but because of the risks, it’s a highly regulated space requiring oversight by an institutional biosafety committee (IBC).

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4 min. read
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Webinar

Privacy and Confidentiality in the Age of Mobile Apps and Connected Devices

Discover how to protect participant privacy in mobile-app-based clinical research. Learn about risks and what IRBs need to consider in protocol review.

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White Paper

Unique First-in-Human Phase I IRB Considerations you Might not Know About

An institutional review board (IRB) may ask some different questions for first-in-human (FIH) Phase I trials than later phase studies.

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Webinar

How to Optimize Your sIRB Experience

Find out how other institutions have used sIRB requirements as an opportunity to elevate their research programs in this webinar.

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Blog

Beginner’s Guide to Single IRB Mandates

More governing bodies are starting to opt for single institutional review board (sIRB) review as a way to streamline research operations.

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5 min. read
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News

Updated Advarra Fee Schedules Now Available

TAdvarra’s updated fee schedules for IRB, IBC, DMC, and EAC are now available. The new fee schedules are effective January 1, 2023.  

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1 min. read
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Blog

Your Guide to sIRB Mandates

sIRB regulations and policies have been announced and implemented to help address the challenges of conducting clinical trials involving multiple research sites.

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4 min. read
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