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Info Sheet

IRB Services for Federal Grants

View this info sheet to learn about Advarra’s IRB expert oversight and guidance to support your next federal grant proposal.

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Info Sheet

Planned Emergency Research: Points to Consider

Download tips and considerations for sponsors and IRBs for next research project involving exception from informed consent (EFIC)

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Blog

Beginner’s Guide to Institutional Review Boards (IRBs)

In the U.S., there is an independent group overseeing clinical research, ensuring participants’ rights and welfare are protected.

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Infographic

What Level of Review Does Your Study Need?

In this infographic, we share useful information for investigators to know which level of IRB review likely applies to their study.

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Info Sheet

IRB Review Services for Cosmetics Research

This info sheet describes Advarra’s specialized expertise, dedicated support, and rapid IRB review timelines for cosmetics research studies

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White Paper

Reporting to the IRB: What Does and Does Not Need to be Reported

This white paper outlines IRB reporting requirements, why reporting is important, and what should and should not be reported.

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Podcast

James Riddle and Willie Muehlhausen Discuss Digital Technology and Virtual Data Collection in Clinical Research

In this episode, we discuss the growth of decentralized clinical trial technology and how IRBs evolved to account for technology advancements.

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Info Sheet

Study Startup Support Info Sheet

Advarra provides flexible solutions that help accelerate the initial IRB review process and make it more efficient.

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Info Sheet

IRB Services for Institutional Site Networks

Download this info sheet to learn more about IRB services for institutional site networks

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Abstract

Navigating the Ethics of Remote Research Data Collection

In this article, Luke Gelinas develops a framework to identify and address key challenges for remote research data collection.

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Infographic

US Medical Device Regulation 101

Speed the review process by understanding how medical devices are classified & what the IRB must review to approve device research.

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Webinar

FWAs Part 2: Managing a Federalwide Assurance and IRB Registration

Join Advarra’s regulatory experts in another discussion of institutional and IRB responsibilities and dig deeper into the FWA topic.

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