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The Killer Issue: How to mitigate risk when designing in-vivo devices

Tuesday 15 September 2020 @ 2:00 pm - 3:00 pm BST

SEHTA & eg technology

Series of In-vivo devices, Microfluidics and Diagnostics Webinars

September 2020

SEHTA 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.

Each session will run for 1 hour:  14:00 – 15:00 (UK time)

These webinars will be run via WEBEX – details on application

Risk goes hand in hand with medical device design and development – intervening in the human body will always have the potential to go wrong. But what happens when device limitations could result in serious injury or even death? Join egt director, Danny Godfrey as he looks specifically at the design and development of in-vivo devices and how risks are identified, managed, and mitigated to minimize the risk of potentially catastrophic outcomes.

Starting with a brief overview of the medical device development process, this webinar will address the importance of examining the full use cycle of your device and identifying risks early on in your project – including less obvious and sometimes unseen obstacles – whilst ensuring full traceability throughout.

Topics to be covered include:

  • The key things to consider from the outset of any development programme
  • How to identify the full spectrum of potential risks
  • When in your programme this should happen
  • The importance of device classification and mapping risks against standards
  • How to mitigate risks to allow you to get on with your design

Target 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.

Costs to attend:

Early bird rate – book by 31st August 2020

£55 + VAT pp per webinar for members / £65 + VAT non-members

After 31st August 2020

£65 +VAT pp per webinar for members / £75 + VAT non members

Not a member of SEHTA – it’s free to join – https://www.sehta.co.uk/Post/sehta-membership

For more information and to book, click here

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