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The primary producers of research data are researchers themselves, although in some cases, data may be generated and deposited automatically from experimental equipment.
The goal of ImmPort is to ensure that basic and clinical research data are accessible to researchers in ways that allow effective sharing of data and knowledge.
Immunology research data are collected and curated in the Private Data application with access controlled by data providers and later published through the Shared Data application for open access.
Other aspects of the research context determining the scope of the researcher's duty to return individual research data are the vulnerability and dependence of the study population; whether a clinical relationship already exists between researcher and participant; the intensity and duration of their interactions; and the availability of adequate funding, personnel, and technology.
It is therefore important that alternatives to traditional methods for collecting, storing and using biomedical and social research data are proposed and consequently exposed to scrutiny by information security experts, researchers and interested members of the general community, alike.
Papers that utilize public data (e.g., Census) or original research data are appropriate for CELS.
High volumes of clinical and drug research data are being generated across the world every day.
This wisdom can also guide the decision process when research data are absent.
Has there been a change in how research data are collected?
Services and expertise related to the management of research data are distributed throughout multiple units at Cornell University.
Similar(1)
Clinical 'care' data are often stored in electronic health records (EHR) or CDW, whereas clinical 'research' data are collected in electronic case report forms or clinical data management systems.
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