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Search results for "FHIR": 1,661 articles

International: 1,661 articles
FHIRInternational🏛(メール詳細から取得可)EnrichedNov 17, 2025

Guide to Setting Up MCP Server for FHIR Integration

This article provides a technical guide on how to set up FHIR integration within the Cline tool. Users must use the provided JSON configuration example, tailored for operating systems like macOS, Windows, or Linux, and input it via the 'Add MCP Server' function. Crucially, restarting Cline is required after completing this setup.

FHIRInternational🏛Google CloudEnrichedNov 15, 2025

How to Patch a DICOM Store using Google Cloud Healthcare API

This article provides detailed instructions and code samples for updating the configuration (Pub/sub topic name) of a DICOM store using the Google Cloud Healthcare API. Developers can modify the notification settings of a DICOM store via API calls using major languages like Go, Java, and Node.js.

Google CloudFHIRDICOMHL7
FHIRInternational🏛(メール詳細から取得可)EnrichedNov 13, 2025

Common Data Models and Data Standards for Tabular Health Data: A Systematic Review

This systematic review systematically evaluates Common Data Models (CDMs) and data standards necessary to integrate diverse data sources and enable federated analysis. The study concludes that OMOP CDM and FHIR scored best across various criteria, emphasizing that achieving seamless interoperability requires enabling transformations between different representations rather than relying on a single global model.

FHIRInternational🏛中央健康保險署 (NHIA)Nov 11, 2025

【亞太醫療永續轉型論壇】AI 協作「以人為本」的醫療轉型:臺日專家聚焦數據標準與臨床流程

2025年アジア太平洋永続医療論壇では、台湾と日本の医療専門家が集結。AIは人間の判断を補佐する「助攻者」であり、単なる代替物ではないという認識で一致した。台湾の健保署や日本大学病院など、各機関がデータ標準化(FHIR等)や低リスクからの導入を通じて人機協働を進める。

FHIRInternational🏛(メール詳細から取得可)EnrichedNov 11, 2025

Latest Trends and Regulatory Compliance Guides for HL7 FHIR in Healthcare Data Interoperability

This article provides guidance on applying the FHIR standard to specific use cases, such as eCTD v4.0 and Veeva CRM/Epic EHR integration. It details solutions for international regulatory requirements and technical challenges in areas like pharmaceutical labeling (e-labeling) and clinical research data (eSource/ePRO).