| DICOM PS3.2 2025a - Conformance |
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[Any important remarks, disclaimers, and general information are specified. The following example may be used as a template.]
The scope of this DICOM Conformance Statement is to facilitate integration between < Product> and other DICOM products. The Conformance Statement should be read and understood in conjunction with the DICOM Standard [1]. DICOM by itself does not guarantee interoperability.
The Conformance Statement does, however, facilitate a first-level comparison for interoperability between different applications supporting compatible DICOM functionality.
This Conformance Statement should not replace validation with other DICOM equipment to ensure proper exchange of intended information. In fact, it is the user's responsibility to perform the following validation activities:
The comparison of Conformance Statements from <Product> and other DICOM conformant equipment is the first step towards assessing interconnectivity and interoperability between those systems.
Test procedures should be defined and executed to validate the required level of interoperability with specific DICOM conformant equipment, as established by the healthcare facility.
[If the product has an IHE Integration Statement, the following statement may be applicable]:
<Product> has participated in an industry-wide testing program sponsored by Integrating the Healthcare Enterprise (IHE). The IHE Integration Statement of <Product> together with the IHE Technical Framework may facilitate the process of validation testing.
| DICOM PS3.2 2025a - Conformance |
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