Resources

Author: Ashley Toy

Ashley Toy

Ashley is the Product Marketing Manager for Forte's Research Evaluation System (EVAL), Electronic Data Capture (EDC) System, Participant Payment System, business intelligence system (Insights), and comparative analytics tool (Benchmarks) products. In addition to assisting with the development of marketing and product strategy, Ashley is an active contributor to Forte's educational resources, including webinars, blog articles, eBooks and more.

Website: Forte

Top 6 Challenges in Informed Consent

Informed consent is important to any clinical trial – but that doesn’t mean it comes without challenges. Read more about the top 6 challenges research institutions face.

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Forte’s Onsemble Conference Builds on the Past and Looks Forward to the Future

As the 2019 Fall Onsemble Conference comes to a close, we are grateful for another successful gathering of our customer community.

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Welcome to the 2019 Fall Onsemble Conference

Members of the Onsemble Community are gathering this week in our hometown of Madison, Wisconsin to learn industry best practices, connect with their peers and celebrate another great year.

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7 Can’t-Miss Sessions at the Fall 2019 Onsemble Conference

Want to know more about the kinds of presentations you’ll see at the conference? Here’s a preview of 7 can’t-miss sessions from each of the different subject focus areas.

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Cancer Research Career Enhancement: The Importance of Education and Training in the CCSG

In order to stay on the cutting edge of their field, researchers need to continue to grow their knowledge and understanding through continued education and training.

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5 Questions to Ask to Ensure Successful Clinical Trial Technology Adoption

When an organization begins the process of rolling out new technology, securing end-user adoption is critical to the success of the system whether it’s a CTMS or an EDC software.

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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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Build or Buy? How the University of Chicago Comprehensive Cancer Center Made the Move to EVAL

Handling all of the data needed to manage an organization’s Cancer Center Support Grant (CCSG) is a difficult task. This is the story of how the University of Chicago Comprehensive Cancer Center adopted industry-leading research administration technology and reallocated their technical resources to higher value projects.

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What is the Common Rule? 5 Helpful Resources to Learn More

While the Common Rule is critical to ensuring the ethical conduct of human subjects research, it can be difficult to navigate the changing requirements. We’ve compiled some helpful resources to assist in getting to know the Common Rule.

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Roles in Clinical Research: The Core Study Team

In this article, we discuss some of the key roles on the research team that are involved in the day to day conduct of a study. While not an exhaustive list, these are some of the core team members that make clinical research happen.

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