Resources

Data Management

Latest Data Management Resources

Beginner’s Guide to Risk-Based Monitoring

In clinical research, there are many different data points to track and monitor as the trial moves from phase to phase. Learn more about risk-based monitoring and how it fits in with clinical trials.

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Wayne State University Streamlines Compliance with Validation Services for Forte EDC

When Wayne State University (WSU) wanted to take on more IND and IDE trials, they chose Forte EDC and Forte’s Validation Service to help streamline the process.

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The Rise of Electronic Data Capture

Traditional paper-based trials are becoming a thing of the past. Learn about the rise of EDC and how it improves clinical trials in this infographic.

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Beginner’s Guide to eSource Data Best Practices

Leveraging technology is essential to successfully streamlining the start-up and conduct of trials. From clinical trial management systems to electronic regulatory management systems, clinical research technology has been instrumental in making improvements in the entire protocol lifecycle.

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Building a Foundation for Quality Clinical Research Data, Reporting and Analytics

In this webinar, members of Forte’s project and product management teams will provide a roadmap to ensure your site is following best practices for collecting and making the best use of your data.

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UChicago Comprehensive Cancer Center Adopts Industry-Leading Technology with EVAL

Learn how UChicago decided to make the move from a custom application to a community and vendor supported solution to manage their research administration data. UCCCC chose to leverage EVAL as their first Forte solution to help streamline their data management processes.

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Tips to Ensure Data Quality When Implementing or Optimizing a CTMS

Creating processes that result in accurate, timely and complete data are invaluable when implementing or optimizing a CTMS. Here are a few tips to achieve your goals.

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Overcome These 5 Common Clinical Trial Challenges Using a CTMS

Learn how a CTMS can help you beat these common struggles and increase productivity at your clinical research site.

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Report Card: Methods for Managing Lab Norms within your EDC System

How varying protocols and operations should change your organization’s approach to handling external data in your EDC system.

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Enhancing Competency with Clinical Research Technologies

Forte and ACRP partnered to conduct a survey analyzing the factors that contribute to technology competency and how sites, technology providers and clinical research professionals can work to improve these competencies across the industry.

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