WhitePapers2018-09-26T02:03:13+00:00

Building Clinical Data Registries (CDRs) that support acquisition, curation, and dissemination of research data poses a number of unique challenges. CDRs must operate within a complex ecology of data sources, consumers, and governance. Prometheus has identified seven informatics challenges that this complex ecology poses for CDRs, the questions you should ask when addressing research data management, and how RexStudy is engineered to ensure your research teams generate high-quality, reliable, and statistically sound data.

Estim. Reading: 15 min

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Online survey websites and smartphones facilitate faster and cheaper collection of large amounts of rich survey data. But these new opportunities come at a cost: faster and cheaper surveying demands greater attention be paid to data integrity. Understand the pros and cons of these methods, the pitfalls that often accompany them, and ways in which survey data can be maximally beneficial for research.

Estim. Reading: 11 min

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There is growing pressure within the scientific community to more fully repurpose existing data. However, the challenges of working with secondary data means researchers must be strategic in their approach. Get a comprehensive overview of the advantages, limitations, best practices, and analytical tools available for conducting secondary data analysis.

Estim. Reading: 10 min

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EHRs can facilitate faster and cheaper clinical research investigations. By collecting diagnostic, intervention, and outcomes data at all levels of care and across time, EHRs capture a richer picture of clinical effects, relationships, efficiency, and more. However, the task of extracting research-grade data from oftentimes fractured EHR databases is non-trivial. Learn how to spot issues and understand your options.

Estim. Reading: 14 min

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In its truest form, automation denotes a process that takes new information as it becomes available, synthesizes it, and makes a decision as to what the appropriate next action should be. Learn how automation is used in clinical research and what effect an integrated data management infrastructure has on the ability to employ automated decision-making.

Estim. Reading: 12 min

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Clinical Data Registries are emerging as one of the best tools for conducting research on quality of care and patient outcomes, but most never realize the full value of the information within their reach. Learn why Data Request Portals (DRPs) offer a new, sustainable revenue channel for registry stakeholders, and the prerequisites, challenges, and pricing models to consider while planning a DRP.

Estim. Reading: 11 min

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