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4 Key Integrations for Your Clinical Trial Management System
Integrating your clinical trial management system enterprise-wide poses many benefits. Learn how your team can further streamline operations.
Ideas for Managing Clinical Trial Finances Post-Pandemic
Learn how effective financial workflows are critical to managing your research in 2021 and beyond thanks to industry changes this past year.
Aidan Gannon and Jessica Perry Examine the Patient-centric Revolution
In this episode, Aidan Gannon of Advarra and Jessica Perry of Moderna discuss patient centricity in clinical research.
Key CTMS Capabilities to Improve Financial Management
This blog outlines what you should look for in a CTMS to maximize your organization’s return on investment.
Effective Clinical Trial Financial Management Post-Pandemic
This eBook investigates shifting fiscal priorities and strategizes how sites can ensure effective financial management post-pandemic.
Why Institutions Should Consider an Externally Administered IBC
Gene therapy clinical trials require specialized oversight & expertise. Read how institutions can prep for the boom in gene therapy research.
Site-Driven Metrics: Operational Data To Improve Research
Most metrics are geared toward sponsors and CROs, find out how this ultimately impacts site research operations
Advarra Announces Key Growth Milestone for The Gene Therapy Ready Network, Becoming Largest IBC Service
Advarra's network has grown to over 500 registered research sites, becomes the largest administrator of institutional biosafety committees
Addressing Barriers to DEI in Clinical Research
A diverse, equitable, & inclusive research environment benefits everyone: trials & the communities alike. How can sites incorporate more DEI?
Q&A from Remote Monitoring: Study Compliance In A Changing World
In a recent webinar, Advarra experts provided insights and information in Remote Monitoring: Study Compliance in a Changing World
The State of Clinical Trial Activation at Sites
While the study activation process is necessary for all sites to conduct, efficiently coordinating all necessary aspects can be challenging.
Regulatory Fine Points: What Research Sites Need to Do for Part 11 Compliance
Summary of James Riddle's Presentation at SQA, which outlines considerations for sponsors when ensuring 21 CFR Part 11 compliance at sites.
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