Most clinical research sites are expected to manage multiple concurrent studies, often with different data types (e.g., administrative, clinical, laboratory) and methods of data capture (e.g., manual entry vs. automatic loading).

But, as more studies and data types are introduced, existing data exploration tools and interfaces become less effective. 

 

The informatics best practice for exploring data across multiple studies and data types is not to build one "query tool to rule them all," but rather to provide "data marts" optimized for specialized uses, so that principal investigators, external collaborators, study coordinators, and internal stakeholders can access the data they need, at the time they need it.

Join us for this complimentary webinar on how clinical researchers are leveraging 'data marts' to more effectively and efficiently explore sensitive data in highly regulated environments.

What You'll Learn

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Challenges of sharing, reusing, and accessing platform-agnostic EDC form configuration

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Overview of the RIOS metadata definition standard and where to access additional resources on RIOS. 

PR_blue_circle_bullet_flame_iconReal world example of RIOS in a multi-site Quality Improvement Initiative.

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Future road map, including plans to integrate RIOS with the Center for Open Science's (COS) Open Science Framework. 

 

ORIGINAL PRESENTATION DATE: July 11, 2016

View this webinar

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Key Information

Open Most clinical research sites are expected to manage multiple concurrent studies, often with different data types (e.g., administrative, clinical, laboratory) and methods of data capture (e.g., manual entry vs. automatic loading). But as more studies and data types are introduced, existing data exploration tools and interfaces become less effective. 

The informatics best practice for exploring data across multiple studies and data types is not to build one "query tool to rule them all," but rather to provide 'data marts' optimized for specialized uses, so that principal investigators, external collaborators, study coordinators, and internal stakeholders can access the data they need, at the time they need it. 

About the Speakers

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Leon Rozenblit, JD, PhD, Founder & CEO

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Frank Farach, PhD, Director of Program Management

"Helpful information provided to better understand the issues and solutions. Clear and concise content."

- Wendy T., Clinical Trials Specialist

"Very interesting webinar; very timely. Gives us the direction in which to move."

- Susan A., Research Coordinator

"Great presentation. I plan on sharing the recording with my coworkers."

-  Eryn B., Certified Clinical Research Coordinator