Research Operations
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.
Advarra Launches New Clinical Research Conduct Training to Streamline Site Activation
Training program leverages research expertise and technology to accelerate study start up by educating principal investigators and site staff.
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.
Driving Site Efficiency and Visibility Using a CTMS
As clinical trials grow more complex, this eBook reviews how a CTMS may help your organization address challenges as you conduct research.
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.
IRB Review of International Research
Advarra’s institutional review board (IRB) can support local ethics committee reviews and confirm compliance with U.S. regulations.
Understanding Various Decentralized Terms in Research
Virtual, remote, hybrid, decentralized, mHealth, telehealth: Find out what these terms mean for clinical research.
Manual Data Migration
Download the info sheet to learn about Advarra’s manual data migration services for various technology platforms.
Budgeting and Billing Compliance in Study Activation
Faced with expanding their budgets, sponsors and sites must enable budgeting and billing compliance best practices starting at study activation.
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.
Duke University Prioritizes Advarra eReg’s Site Centric Workflows within a Connected Research Ecosystem
Download the case study to learn more about how Advarra eReg’s site centric workflows streamlined Duke University’s clinical operations.
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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