04 Feb 2021Ended

Software UKCA Marking Webinar


Estimated Turnout

upto 100
Based on previous editions


Feb 2021


Not Available
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The UKCA (UK Conformity Assessed) Marking is a new UK product marking that will be used for goods being placed on the market in Great Britain (.. Read more England, Wales and Scotland). It covers most goods which previously required the CE Marking, including medical devices and in vitro diagnostics. Target audience:  Manufacturers based outside of the UK wanting to access the UK market, UK based manufacturers wanting to access the EU market, 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.

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South East Health Technologies Alliance

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