Blog

This blog offers practical tips for effective site training to ensure your global clinical trials are compliant and efficient.

Find out how Advarra's approach to the SDLC lifecycle leads to successful collaborations among sites and sponsors.

Here are four questions to ask during the selection process to offer more insight into your future success with the selected vendor.

Find out how to address Phase I research challenges to enable efficient IRB review and timely study startup.

Ensure your organization has the tools to both efficiently and compliantly implement remote modalities to best reap the benefits of DCT

eSource, ePRO, and EDC are integral to efficient clinical research. This blog explores how they work together and their differences.

How can researchers know when research is minimal risk? Learn an overview and the regulatory flexibilities that might be eligible.

Learn more about independent asset reviews and how they can enhance research operations.

This blog describes the difference between medical science liaisons and clinical liaisons, and their role in clinical research.

Explore how the COVID-19 pandemic has changed the clinical trial landscape and how it affects the business pipeline.

Integrating your clinical trial management system enterprise-wide poses many benefits. Learn how your team can further streamline operations.

Understand a data strategy's role in clinical research and how enforcing one will benefit your studies.