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Medical Hectic GmbHmediCAD 5.0 / median 1.84 DI COM Conformance StatementSeite: Datum:1 on 10 13.11.20171. Introduction 1.1PurposeThis DI COM Conformance Statement is written according to part PS
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To fill out this DICOM conformance statement, follow these steps:
02
Gather all the necessary technical information related to the equipment or software being described in the conformance statement.
03
Start by providing an overall description of the system, including its purpose and functionality.
04
Specify the DICOM conformance statement level for the system, such as Application, Communication, or Archive.
05
Identify the DICOM services supported by the system, such as Storage, Query/Retrieve, or Print.
06
Provide detailed information about each supported DICOM service, including service class, SCU/SCP role, and related implementation details.
07
Document any system-specific restrictions or limitations that may affect the conformance of the system to the DICOM standard.
08
Include any necessary vendor-specific conformance requirements or extensions.
09
Review and update the conformance statement regularly to reflect any changes or updates to the system.
10
Validate the completed conformance statement against the DICOM standards using appropriate validation tools.
11
Distribute the finalized conformance statement to relevant stakeholders, such as customers, regulatory authorities, and vendors.

Who needs this dicom conformance statement?

01
The DICOM conformance statement is needed by manufacturers, developers, and suppliers of medical imaging equipment, software, and related services.
02
It is also required by healthcare providers or institutions implementing DICOM-based systems for the purpose of interoperability and compliance with industry standards.
03
Medical imaging professionals, such as radiologists and technologists, may also refer to the conformance statement to understand the capabilities and limitations of the imaging systems they use.
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A DICOM conformance statement is a document that describes how a DICOM-compliant device or software application operates in relation to the DICOM standards.
Manufacturers of medical imaging devices and software that create, store, or transmit DICOM images are required to file a DICOM conformance statement.
To fill out a DICOM conformance statement, the manufacturer should follow the DICOM Conformance Statement Template and provide details about the implementation, supported services, and any specific functionality.
The purpose of a DICOM conformance statement is to inform users and other developers about the capabilities, limitations, and interoperability features of a DICOM product.
Information reported in a DICOM conformance statement typically includes product identification, supported DICOM services, implementation details, and any deviations from the standard.
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