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Webinar

Current State of Site-Sponsor-CRO Collaboration

Upcoming: February 27

View the Current State of Site-Sponsor-CRO Collaboration webinar to learn about survey findings, improve communication, and optimize clinical trial efficiency.

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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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5 min. read
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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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5 min. read
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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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5 min. read
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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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6 min. read
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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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5 min. read
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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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