Data Management

Latest Data Management Resources

Ensuring Quality in Risk-Based Monitoring and Data Protection

Protecting participant data is of the utmost importance in clinical research. This article breaks down risk-based monitoring, as well as other data protection terms falling underneath it.

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Q&A: How Sites and Sponsors are Collaborating to Move eSource Forward

In this Q&A, Shannon Roznoski from Advarra-Forte and Michael Buckley from Memorial Sloan Kettering Cancer Center answer attendee questions from their webinar, How Sites and Sponsors are Collaborating to Move eSource Forward

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Better Together: Site and Sponsor Collaboration to Revolutionize eSource in Clinical Trials 

By inverting the focus from per protocol solutions to holistic site-wide solutions that utilize industry standards, we can revolutionize the use of eSource in clinical trials.

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Preview: Forte’s Pre-Conference Workshop at CCAF 2020

At this year’s CCAF conference, we will host a pre-conference workshop, “Research Administration Technology Workshop”, allowing us to work collaboratively with the clinical research community.

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The Beginner’s Guide to Implementing an Enterprise eRegulatory Management System

Many sites understand the benefits of moving from paper regulatory binders to an electronic system. But it’s also important to ensure your organization is implementing a system that will fit your regulatory workflows and set you up for long-term success.

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Reflections on SCDM 2019: Technology’s Role in Transforming Clinical Data Management

Forte’s director of product management attended the SCDM Annual Conference earlier this month, and took the time to reflect on the growth of the clinical data management domain.

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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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