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FDA Regulations on Medical Devices How to Penetrate the US Market TEMPLATES Copy before use

FDA Regulations on Medical Devices: How to Penetrate the US Market

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InnoScot Health and Heriot-Watt University are set to link up once again to deliver webinar learnings around successfully achieving Stateside medical device compliance

InnoScot Health’s Head of Regulatory Affairs Elaine Gemmell and Professor Marc Desmulliez, Manager of the MDMC will help to lead a free online webinar entitled FDA Regulations on Medical Devices: How to Penetrate the US Market which is taking place on Friday 24 November at 10am.

The workshop – run by MDMC and Scottish Enterprise – will be hosted on Microsoft Teams with a link provided to attendees following registration.

Interested parties can alternatively opt to take part in the same interactive workshop held on two other dates next year – Wednesday 24 January and Wednesday 21 February.

A woman taking part in a webinar on her laptop.

Register to Attend

All three deep dive sessions will feature speakers Elaine – awarded the title of Honorary Professor of the School of Engineering and Physical Science at Heriot-Watt University earlier this year – and Marc, as well as Principal Consultant at Compliance Solutions (Lifesciences) Ltd, Edwin Lindsay.


The trio will be presenting an introduction to navigating medical device regulation as it stands in the UK and Europe, before shifting their focus to the demands of the United States’ Food and Drug Administration (FDA) where there are similarities but also significant differences for those looking to commercialise their products.

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