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Blog

Budgeting for IRB Review: A Guide for HRPP Leadership

Internal IRB reviews are NOT free, contrary to popular belief. In this blog we outline practical steps for assessing and establishing IRB review cost

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E-Book

Empowering Clinical Trials: The Pivotal Role of eSource

Our eBook outlines how eSource can make clinical research data more accessible, accurate, and reliable.

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White Paper

4 KPIs Clinical Research Study Managers Can Master

This white paper examines four KPIs most impacting timelines and budgets and offers strategies for effective communication and risk mitigation.

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Blog

Clinical Trial Efficiency: Top Risk Indicators and Solutions for Site Performance

Monitor four critical metrics across your sites to prevent persistent challenges to clinical trials

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Blog

Our OnCore CTMS Vision: Building a Foundation for Success

More than two decades ago, we created OnCore CTMS. What do we have in store for the future?

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White Paper

Operationalizing Research Analytics: Today, Tomorrow, Someday

Uncover how analytics, artificial intelligence, and machine learning are reshaping the foundational elements of clinical research.

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E-Book

Unlocking Study Activation: 2023 Study Activation Report

Access the survey report now for current perspectives on study startup activities impacted by rapidly evolving technology and tools.

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Blog

What is a Data Monitoring Committee?

In a complex clinical trial, data monitoring committees oversee interim data to ensure adequate safety monitoring.

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Blog

Improving Study Activation Time for Gene Therapy Research

With the growing popularity of gene therapy research and genetically engineered vaccines, sites need to understand study activation impacts

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White Paper

4 Modernized Functions Every Sponsor Needs for Study Startup

This white paper outlines four technology capabilities sponsors need to expedite the study startup process.

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White Paper

Data on the go: Mobile Application Considerations for Clinical Trials and Beyond

Find out the necessary regulatory and ethical considerations when utilizing an app or connected device in human subjects research.

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Case Study

University of Nebraska Medical Center Streamlines Regulatory Management and Accelerates Study Startup with Advarra eReg

Learn how Advarra eReg helps UNMC support remote monitoring and how eReg helped address prevalent challenges in clinical research.

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