Technology
3 Must-Haves to Deploy Remote Clinical Trials
Ensure your organization has the tools to both efficiently and compliantly implement remote modalities to best reap the benefits of DCT
Understanding eSource, ePRO, and EDC
eSource, ePRO, and EDC are integral to efficient clinical research. This blog explores how they work together and their differences.
Understanding Medical Science Liaisons and Clinical Liaisons
This blog describes the difference between medical science liaisons and clinical liaisons, and their role in clinical research.
Maintaining a Robust Clinical Trial Pipeline
Explore how the COVID-19 pandemic has changed the clinical trial landscape and how it affects the business pipeline.
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.
How to Design Digital Materials for Participant Engagement
Keeping a participant informed and engaged in any study is critical. This blog outlines how we can engage participants digitally.
Diversity and Inclusion: Who is Responsible – Site, CRO or Sponsor?
Register for our webinar for a discussion on why it’s important to recruit diverse patients of all backgrounds.
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.
Beginner’s Guide to IND Safety Reporting Under 21 CFR 312(c)
Learn how to ensure compliance with FDA 21 CFR 312.32, and explore Advarra solutions that support efficient and compliant safety reporting.
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