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SUMMARY:Diagnosing the risk in diagnostics development; man versus machine
DESCRIPTION:Series of In-vivo devices\, Microfluidics and Diagnostics Webinars \nSeptember 2020 \nSEHTA and eg technology are delighted to announce a series of webinars on the topics of In-vivo devices\, Microfluidics and Diagnostics to enable you to continue to update your skillset and move your medical technologies and companies forward. \nEach session will run for 1 hour:  14:00 – 15:00 (UK time) \nThese webinars will be run via WEBEX – details on application \nThe design and development of Diagnostic devices within the medical industry is a complex process\, fraught with usability uncertainties. Many clinicians are reluctant to make a diagnosis without the confirmation of a device\, but devices cannot always be used in isolation as they do not have the full picture and patient knowledge of the clinician. This dichotomy makes the development of such devices often difficult. So\, how do we develop a diagnostics device which satisfies the product\, patient\, and clinician requirement specifications? Furthermore\, how can we develop a diagnostics strategy that addresses the codependence of diagnostic devices and their user? \nThis webinar will focus on what it takes to produce a diagnostics device which not only meets requirements but lives up to its marketing. Looking at the user and usability requirements\, how your device should be classified and the importance of creating a defined strategy\, we will discuss the human factors involved with diagnostics design and how total reliance on the device is not always the best option.  \nTopics to be covered include: \n\nThe key considerations in a diagnostics device development programme\nThe importance of identifying your product strategy early in your programme\nHow to keep usability and the end-user in mind throughout\nNavigating the regulatory process\nClosing the design loop – ensuring your end product does what you say it does!\n\nTarget audience for these webinars are: Medical Technology Entrepreneurs\, Medical Device Software Developers\, Technology Transfer Officers\, Medical Technology University Researchers\, IVD Developers\, Business Owners\, Executives\, Product Owners\, Regulatory Specialists within a company that need to understand the overall regulatory requirements for their medical devices to enable them to place a device on the market and to maintain access. All company sizes will find it useful. \nCosts to attend: \nEarly bird rate – book by 31st August 2020 \n£55 + VAT pp per webinar for members / £65 + VAT non-members \nAfter 31st August 2020 \n£65 +VAT pp per webinar for members / £75 + VAT non members \nNot a member of SEHTA – it’s free to join – https://www.sehta.co.uk/Post/sehta-membership \nFor more details\, and to book your place\, click here
URL:https://staging.medilinkmidlands.com/event/diagnosing-the-risk-in-diagnostics-development-man-versus-machine/
CATEGORIES:Medilink Partner Event
ORGANIZER;CN="SEHTA":MAILTO:info@sehta.co.uk
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