Research Operations
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.
Creating Opportunities for Inclusion, Diversity, Equity and Access In Clinical Research: A Discussion with Tiffany Danielle Pineda, Brian Sevier, and Wendy Tate
About the Advarra In Conversations With… The future of healthcare innovation hinges on research and clinical trials. Advarra sits down...
Implementing Site-Centric Technology to Effectively Manage Your Clinical Trials
This webinar provides an overview of the benefits of adopting new clinical research technologies (focusing primarily on a CTMS).
Effectively Working with a Research Technology Vendor During Implementation
Maintaining an effective partnership with your technology vendor is key to implementation success.
Decentralized Clinical Trials: Growing Trend? Tips and Best Practices for Sponsors/CROs
This webinar will present provide tips and best practices on the growing Decentralized Clinical Trials for Sponsors and CROs
Advarra Trend Report: Analyzing Sites by Organization Type
Clinical Research Workforce survey finds sites once had similar habits, but everyone is approaching the "next normal" differently.
The ROI of Site-Centric Training and Support
Download our white paper to learn how to maximize your research investment for site-centric training and support.
Maintaining Data & Reporting Integrity with Mobile Health
Understand how to properly handle and evaluate incoming data gathered using mobile health (mHealth) apps and technologies.
Integrating Expert Opinions: Why Your Clinical Trial Needs an EAC
In this webinar, we discuss the role of independent endpoint adjudication committees, from charter creation through end of study closeout.
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