Entries by heaventree

Health Innovation Hub Ireland selects KEWS300

Health Innovation Hub Ireland ( www.HIH.ie ) has recognised Syncrophi’s KEWS300 product for its potential to make a real impact within Ireland’s public healthcare system, the HSE. They are assigning a Project Manager to oversee a structured implementation in a targeted public hospital as a reference site.

NSAI re-certifies Syncrophi’s medical-grade quality system yet again

Once again Syncrophi Systems Ltd has achieved a clean bill of health during the annual 2-day audit of our ISO13485 (2012) by our Notified Body, the National Standards Authority of Ireland. This continues our unbroken series of successful assessments since we were first certified in 2008 and underscores our core commitment to medical-grade quality systems.

African health system leaders hosted by Syncrophi

Syncrophi was delighted to host a visit to Galway of the hospital leadership group from South Africa and Kenya who were in Ireland as part of an Enterprise Ireland trade mission. They had the opportunity to see a site-wide example of the use of KEWS300 in a modern hospital setting in the Galway Clinic. A […]

Syncrophi team delivers major software system to Diginewb project consortium

The Syncrophi development team led by Syncrophi Technical Director, Prof. Gerry Lyons, attended the Horizon2020 Diginewb project team bi-annual meeting in Tampere, Finland. The Syncrophi team delivered its first major milestone for this important project: a complete, working prototype which will provide the framework for the project researchers to carry out in-hospital clinical work. http://www.digi-newb.eu/

Northwell Health executive reviews KEWS300 installation

Reference site visit by Elaine Brennan, Managing Director of Northwell’s venture group reviewed the application of KEWS300 at a HIMSS-6 certified facility. A very useful visit which included on-ward demonstrations and user discussions plus senior executive perspectives. Further engagement is planned.

KEWS300 now FDA-cleared

Today we received final confirmation from FDA that KEWS300 is cleared for sale within the US. The user-centered design and extensive software validations, independently certified to the medical device software standard (ISO62304), allow us to offer this system to US-based customers with real confidence.