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. 2010 Dec;8(4):251-9.
doi: 10.1007/s12021-010-9072-z.

Integrating clinical trial imaging data resources using service-oriented architecture and grid computing

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Integrating clinical trial imaging data resources using service-oriented architecture and grid computing

Stefan Baumann El-Ghatta et al. Neuroinformatics. 2010 Dec.

Abstract

Clinical trials which use imaging typically require data management and workflow integration across several parties. We identify opportunities for all parties involved to realize benefits with a modular interoperability model based on service-oriented architecture and grid computing principles. We discuss middleware products for implementation of this model, and propose caGrid as an ideal candidate due to its healthcare focus; free, open source license; and mature developer tools and support.

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Figures

Fig. 1
Fig. 1
Standard workflow for a clinical trial using imaging
Fig. 2
Fig. 2
Potential data flow and distribution of services in an SOA enabled workflow
Fig. 3
Fig. 3
“The fourth eSDI scenario for extraction of data from electronic health records with verification by the investigator” (CDISC 2006)

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References

    1. Clinical Data Interchange Standards Consortium, Electronic Source Data Interchange (eSDI) Group. (2006). Leveraging the CDISC Standards to Facilitate the Use of Electronic Source Data within Clinical Trials. Version 1.0.
    1. FDA. (1997). 21 CFR Part 11: Electronic Records; Electronic Signatures; Final Rule, Federal Register, Washington, DC.
    1. International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH). (1996). ICH Harmonised Tripartite Guideline, Guideline for Good Clinical Practice E6(R1).
    1. Oster, S., Langella, S., Hastings, S., Ervin, D., Madduri, R., Phillips, J. et al. (2008). caGrid 1.0: An enterprise grid infrastructure for biomedical research. Journal of the American Medical Informatics Association, 15, 138–149. - PMC - PubMed
    1. Seifert, P. (2009). IHE Radiology Technical Framework Supplement—Cross-Enterprise Document Sharing for Imaging (XDS-I.b) Integration Profile, Trial Implementation, Rev. 1.1 - 2009-06-21, IHE International.