000107 - Agfa HealthCare

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Page 6 of 25MED/RLR/000107Document No. 000107, Revision 3.111 September, 2000 Agfa Medical ImagingRevision RecordRevisionNumberDate Author Reason for Change1.0 30/9/96 Eric Initial release1.1 27/01/99 Amorris Company name changed2.0 10/03/99 Wrose Figure 1 to be corrected2.1 10/03/99 Wrose Extra revision created to solve copying problem2.2 10/03/99 Wrose Figure 1 corrected2.3 9/07/99 Amorris New introduction incorporated2.4 22/12/99 Amorris New style implemented2.5 18/1/00 Amorris Returned to old style2.6 16/2/00 Amorris Release 3.5 indicated in title and text; Released 16.2.002.7 16/2/00 Amorris Post-release correction2.8 8/03/00 Amorris Re-imported into mPower3.0 8/9/00 Kkeller New conventions to be implemented3.1 8/9/00 Kkeller New conventions implementedA]
MED/RLR/000107 Page 7 of 25Document No. 000107, Revision 3.1Agfa Medical Imaging 11 September, 20001 INTRODUCTION1.1 Intended AudienceThe user of this document is involved with system integration and/or software design. We assume that thereader is familiar with the terminology and concepts that are used in the DICOM 3.0 standard.Readers not familiar with DICOM 3.0 terminology should first read the appropriate parts of the DICOMstandard itself, prior to reading this conformance statement.Although the use of this conformance statement in conjunction with the DICOM 3.0 standard is intended tofacilitate communication with other imaging equipment, it is not sufficient to guarantee, by itself, the interoperationof the connection. The following issues need to be considered:1.1.1 IntegrationThe integration of any device into a system of interconnected devices goes beyond the scope of theDICOM 3.0 standard and this conformance statement when interoperability is desired. The responsibility foranalyzing the applications requirements and developing a solution that integrates the Agfa equipment withother vendors’ systems is the user’s responsibility and should not be underestimated.1.1.2 ValidationTesting the complete range of possibilities between the Agfa equipment and non-Agfa devices, before theconnection is declared operational, is deemed to be a necessity. The user should ensure that any non-Agfaprovider accepts full responsibility for all validation required for their connection with the Agfa equipment. Theaccuracy of image data once it has crossed the interface between the Agfa equipment and the non-Agfadevice as well as the stability of the image data for the intended applications is the responsibility of the non-Agfa provider.1.1.3 Future EvolutionAs the DICOM 3.0 standard evolves to meet the user’s growing requirements and to incorporate newfeatures and technologies, Agfa will follow the evolution of the standard. This evolution of the standard mayrequire changes to devices that have implemented DICOM 3.0. The user should ensure that any non-Agfaprovider who connects with Agfa devices also plans future evolution of the DICOM standard. A refusal to doso may reflect in the loss of functionality and/or connectivity between the different products.1.2 Purpose of this DocumentThis document is a provisional DICOM Conformance Statement for the HIS/RIS services of ImpaxRelease 3.5.Impax is a DICOM service class user for the following service classes: Patient Management, StudyManagement, Results Management, and Basic Worklist Management. Impax both issues DICOM requestsand accepts DICOM events.A]
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000107 - Agfa HealthCare

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