Resources

Clinical Research Technologies

Clinical Research Technologies

AACI-CRI 2019: Working Together to Improve Cancer Clinical Trial Outcomes

The 11th annual AACI-CRI conference is quickly approaching, drawing academic clinical research leaders from across the country. We preview some of the key focus areas of the 2019 conference.

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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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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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Enterprise Research Software: Evaluating Your True Cost of Ownership

Three key reasons why vendor-provided hosting and infrastructure could be a more sustainable solution for your clinical research software.

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Easing the Struggle of Implementing of Large-Scale Changes at Your Institution

Implementing change can be a difficult and time-consuming experience for clinical research leadership. Here are a few tips to make the transition easier for your teams.

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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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Clinical Trials Day: Tips to Retain Your Clinical Research Coordinators

This Clinical Trials Day, we want to celebrate the contribution made by your clinical research coordinators, and provide actionable ways to provide them with a fulfilling work environment.

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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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Creating new efficiencies through multi-site regulatory data exchange

Coordinating centers  often struggle with the administrative burden of managing regulatory documents across multiple participating sites. We collaborated with our customers to address this challenge through the Forte eRegulatory Management 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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