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News Release from: Cynllun Trosolwg
Edited by the Manufacturingtalk Editorial
Team on 05 January 2007
Software engineering for medical devices
MDT conference seminar examines approaches to software engineering within regulatory structures for medical devices
The challenges of engineering software for the medical devices industry are examined in a seminar to be held at the MDT Conference (the new Medtec) on 14th February 2007 at the NEC, Birmingham The seminar will be presented by Dr Dave Jennings, founder and director of Cynllun Trosolwg, the software engineering and design specialist based in South West Wales
This article was originally published on Manufacturingtalk on 17 Oct 2006 at 8.00am (UK)
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Creating software for quality, costed products.
A seminar entitled 'From requirements to code seamlessly - Producing what it says on the tin' will be presented at the next IT Wales Business Club event.
"The regulatory framework surrounding medical device development can be a daunting prospect for companies," says Dr Dave Jennings, "However, with the right tools and the right approach, products can be taken to market on time, with predictable quality".
'Software Engineering Challenges and Solutions for Medical Devices' will consider the regulatory framework within which software for medical devices must be produced and describe appropriate development processes that fully meet the standards required.
The seminar will also examine how modern software tools - such as those used by Cynllun Trosolwg - greatly facilitate compliance with the standards to deliver the right software on time and within budget.
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