Research Operations
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.
Integrate Advarra’s CIRBI Platform and your electronic master file (eTMF) via Advarra Connect
Enabling Advarra Connect improves efficiency, reduces administrative burden, and streamlines audit readiness across your research portfolio.
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.
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?
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.
Unique Ethical Issues in Phase I Oncology Studies
An essential step in research, Phase I oncology studies raise unique ethical challenges for sponsors, investigators, and IRBs.
Returning to In-person Work: Sponsor Versus Site Viewpoints
An Advarra Trend Report found sites and sponsors alike are facing shifts as they continue to navigate the pandemic.
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