Research Operations
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.
Developing an Emergency Preparedness Plan for your HRPP
Emergency preparedness plans help institutions plan, prepare for, and respond to emergencies as they arise.
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.
Considerations for Transitioning from Paper to eSource
Explore the benefits of switching from paper to eSource, tips for implementation, and how to maintain compliance.
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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