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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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Blog

Critical Steps for Writing an Impactful Clinical Audit Report

In this blog, we share tips and best practices for writing an impactful clinical audit report.

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5 min. read
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Blog

The Advantages of Outsourcing IRB and IBC Reviews to One Partner

By utilizing a vendor that offers both IRB and IBC services in-house, sponsors can streamline reviews and enhance study startup timelines.

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3 min. read
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Blog

Understanding Various Decentralized Terms in Research

Virtual, remote, hybrid, decentralized, mHealth, telehealth: Find out what these terms mean for clinical research.

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4 min. read
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Case Study

GDPR Implementation Support

Learn how Advarra’s global consulting expertise enabled iSpecimen to implement GDPR with no service interruption to their customers.

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E-Book

Improving Site-Sponsor Relationships: Proactive Strategies for Transparent Clinical Trials 

This eBook outlines how clinical research sites and sponsors can effectively work together to improve their relationship.

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Blog

Navigating the FDA Emergency Use Filing Process

Partnering with Advarra, one nonprofit successfully obtained an Emergency Use Authorization from the FDA within five weeks.

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3 min. read
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Webinar

Didn’t Expect that to Happen: Events that must be Reported Promptly to the IRB

This webinar helps researchers better understand how to evaluate potentially reportable events and what needs to be reported to the IRB.

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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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Blog

Improving Patient Centricity and Research Access

There is an increasing challenge to find eligible patients and build trial awareness, so how should the industry address them?

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3 min. read
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Blog

For FDA Inspection Readiness, Accountability is Key

An Advarra expert provides insight in this Q&A session on the FDA inspection readiness process, including how to improve current workflows.

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3 min. read
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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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