Data Management in Clinical Research

Data capture methods in clinical trials, tips for streamlining the collection and review of clinical data, creating case report forms, and more.

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

June 1st, 2017 by Shannon Roznoski

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

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CTMS-EMR Integrations: Maximizing the Value of Your Systems

April 26th, 2017 by Ryan Monte

Integrating your clinical trial management system and electronic medical record can improve your workflows, patient safety and more.

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5 Steps to Follow When Shopping for a Validated EDC System

April 18th, 2017 by Shannon Roznoski

Shopping for a validated EDC system can seem like a daunting task. Learn five steps that make the process less confusing.

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Revenue Forecast: A Key Performance Indicator for Research Sites

February 28th, 2017 by Kayla Leverton

Learn the right clinical trial data to track consistently to make assembling revenue forecast reports easier for your clinical research site.

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5 Ways to Sell EDC to a Skeptic

February 22nd, 2017 by Tami Haas

Ready for an EDC system? Use these five points to generate buy-in from your leadership team.

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Improving the Clinical Research Industry's Response to Epidemics

November 10th, 2016 by April Schultz

Conference presenters discuss methods for improving the clinical research industry's response to global health concerns like Ebola and Zika.

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Getting Serious About Measuring Your Research Outcomes

October 20th, 2016 by Ryan Monte

As the clinical research industry moves towards more advanced metrics, a research evaluation and reporting system can save time and money, while also providing added visibility into the return on your organization’s investments.

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How EDC Could Save Your Clinical Trial in a Disaster

September 6th, 2016 by Tami Haas

A disaster preparedness plan is key to ensuring unforeseen hazards won’t impact your trial. Make sure your EDC system is included in your plan.

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How to Use CDASH Controlled Terminology

July 29th, 2016 by Shannon Roznoski

Shannon Roznoski of Forte discusses controlled terminology and the uses of these standardized lists of terminology.

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How Transparency Will Lead to Industry-Wide Collaboration in Clinical Research

July 19th, 2016 by April Schultz

To meet industry goals, transparent communication and collaboration need to be a greater focus for stakeholders in clinical research.

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