• Proceedings of the Korea Water Resources Association Conference
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• 2005.09a
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• pp.157-159
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• 2005

• Proceedings of the Korea Water Resources Association Conference
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• 2005.09a
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• pp.42-43
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• 2005

• Proceedings of the Korea Water Resources Association Conference
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• 2005.09a
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• pp.174-175
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• 2005

• Proceedings of the Korea Water Resources Association Conference
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• 2005.09a
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• pp.176-177
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• 2005

• Proceedings of the Korea Water Resources Association Conference
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• 2005.09a
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• pp.804-805
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• 2005

• Proceedings of the Korea Information Processing Society Conference
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• 2012.11a
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• pp.796-798
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• 2012

IHE(Integrating the Healthcare Enterprise)에서는 환자의 전자진료기록 공유를 위하여 XDS.b(Cross-Enterprise Document Sharing.b) 프로파일을 개발하였다. 그러나 XDS.b 프로파일의 Document Source와 Document Consumer는 모바일 환경에서는 사용하기에는 부적당하기 때문에 모바일 환경에서 XDS.b infrastructure에 쉽게 접근할 수 있는 MHD(Mobile access to Health Documents) 프로파일을 개발하였다. 본 논문에서는 전자진료기록 표준인 HL7 CDA 문서 등록을 위한 XDS.b Document Source의 Provide and Register Document Set-b[ITI-41] 트랜잭션과 MHD Document Source의 Put Document Dossier[ITI-65] 트랜잭션을 모바일 환경에서 구현하고 메시지의 크기를 비교하였다. 구현된 결과를 통하여 MHD ITI-65 트랜잭션의 메시지 크기가 XDS.b ITI-41 트랜잭션 메시지 보다 80% 정도 감소함을 알 수 있었다.

• Proceedings of the Korea Information Processing Society Conference
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• 2013.11a
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• pp.298-300
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• 2013

IHE(Integrating the Healthcare Enterprise)의 XDS.b(Cross-Enterprise Document Sharing.b) 프로파일은 의료기관간 환자의 전자진료기록을 공유하기 위해 개발되었으나 모바일 환경을 고려하지 않았다. 이를 보완하고자 IHE에서는 모바일기기에서도 전자진료기록을 공유할 수 있는 MHD(Mobile access to Health Documents) 프로파일을 개발했다. XDS.b 메타데이터는 ebXML(electronic business XML)을 사용하고 MHD 메타데이터는 JSON(JavaScript Object Notation)을 사용하므로 MHD와 XDS.b를 연동하기 위해서는 MHD 메타데이터를 XDS.b 메타데이터로 변환이 필요하다. 본 논문에서는 MHD 메타데이터를 XDS.b 메타데이터로 변환하는 규칙을 정의했다.

• Proceedings of the Korea Water Resources Association Conference
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• 2005.09a
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• pp.753-754
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• 2005

• KSII Transactions on Internet and Information Systems (TIIS)
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• v.12 no.4
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• pp.1396-1414
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• 2018

With the proliferation of the Internet of Things (IoT) healthcare devices, significant interoperability issue arises where devices use proprietary data transfer protocols. The IHE PCD-01 standard has been suggested for the exchange of healthcare data in ISO/IEEE 11073 PHD data model. However, the PCD-01 is not efficient to be used in the IoT environment. This is because the use of SOAP for PCD-01 may be too complex to be implemented in the resource-constrained IoT healthcare devices. In this paper, we have designed a communication system to implement ISO/IEEE 11073 and IHE PCD-01 integration using the IETF CoAP. More specifically, we have designed the architecture and procedures, using CoAP, to seamlessly transmit the bio-signal from the tiny resource-constrained IoT healthcare devices to the server in a standardized way. We have also built the agent, gateway, and PCD-01 interface at the server, all of which are using the CoAP as a communication protocol. In order to evaluate the performance of the proposed system, we have used the PCD data to be transmitted over CoAP, MQTT, and HTTP. The evaluation of the system performance shows that the use of CoAP results in faster transaction and lesser cost than other protocols, with less battery power consumption.

• International Journal of Computer Science & Network Security
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• v.22 no.1
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• pp.39-48
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• 2022

Today the regulation of socio-economic development has been the subject of active scientific debate. The modern paradigm of regulatory policy in foreign countries involves a change in the role and strategy of the state, which determines the relevance of this topic. The aim of the article is to study the current state of regulatory policy research. The article is based on a bibliographic analysis of the study of regulatory policy. The study is based on the data search functions of the Scopus platform. It uses a set of VOSviewer program, online visualization of keywords in the titles of scientific journals and citations of publications. The study led to the conclusion that the number of publications that directly study the nature and features of regulatory policy is insignificant, but constantly growing. In our opinion, further research should determine the essence of regulatory policy as a separate category, a description of its features and factors of formation. It is also necessary to develop a common concept that governments should be actively involved in ensuring the quality of regulation, rather than responding to the shortcomings of regulation, which is evolving into regulatory governance.