Enabling innovation to change healthcare

ICE Standard: Integrated Clinical Environment

ICE Standard: Integrated Clinical Environment Date: 2004–PresentCollaborators: ASTM, AAMI Scope and Purpose of ICE Interdisciplinary meetings convened by the MD PnP program from 2004–2008 (described on this web site) identified key capabilities of a patient-centric integrated clinical environment. These capabilities, such as comprehensive data acquisition for the EMR and the integration of devices to enable …

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MD FIRE Date: October 16, 2008 – PesentCollaborators: Massachusetts General Hospital, Mass General Brigham, Kaiser Permanente, Johns Hopkins Medicine, US Department of Veterans Affairs, American Society of Anesthesiologists MD FIRE: Medical Device “Free Interoperability Requirements for the Enterprise” Medical Device “Free Interoperability Requirements for the Enterprise” (MD FIRE) comprises a white paper and sample RFP …

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FDA Workshops

FDA Workshop Date: January 25–27, 2010Historical Perspective: This FDA workshop was a seminal event in the medical device interoperability timeline. It was the result of a collaboration between: The FDA, the Continua Healthcare Alliance, the Center for Integration of Medicine & Innovative Technology (CIMIT), and the MD PnP Program The FDA (CDRH) Workshop on Medical Device …

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OpenICE The MD PnP Program has developed an open source implementation of the Integrated Clinical Environment (ICE) standard as described in ASTM 2761-09(2013) and made it freely available on SourceForge. The platform consists of software device adapters for medical devices (including anesthesia machines, ventilators, and patient monitors), OMG DDS standard middleware, and demonstration applications. Research …

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MDIDS (Medical Device Interface Data Sheets)

MDIDS (Medical Device Interface Data Sheets) We are developing a reference compendium of medical device interface capabilities and data elements which could enable more complete, effective, and safe device integration. This compendium, which we call Medical Device Interface Data Sheets (MDIDS) will serve as a reference for standards development organizations (SDOs), manufacturers, researchers, and clinical …

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CSR (Clinical Scenario Repository) The CSR is a tool to elicit and document clinical situations in which improved technologies – especially those enabled through Integrated Clinical Environments – could improve patient safety and clinical care. The CSR repository documents situations with potential or actual patient harm as well as hypothetical situations where a clinician or …

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