Translate MedTech – Regulatory Affairs for Medical Devices

Translate MedTech – Regulatory Affairs for Medical Devices

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If for any reason you find that you are unable to attend, please let us know [(0113) 34 37244; email]. Failure to take up a pre-booked place without letting us know with at least 48hours notice will be charged £45 to cover course costs.

This course is an introduction to medical devices and the regulatory requirements for placing medical devices on the market.

About this event

This course, delivered as two 3-hour sessions across two separate days, is an introduction to medical devices and the regulatory requirements for placing medical devices on the market and CE marking of devices. It will help you to understand the regulatory path to CE marking a device, deciphering all the regulatory jargon and understanding the new Medical Device Regulations in Europe as well as the UK legislation.

By the end of the course, you should be well set up to understand the requirements and responsibilities and plan your organisation’s regulatory and clinical strategy. As well as guiding you through the regulations, it brings you up to scratch with all the other relevant guidance, standards and the new Medical Device Regulations both in Europe and the UK.

Open to academics, researchers, clinicians and industry representatives, by attending the course you will:

• Learn about the NEW Medical Devices Regulation Implemented in Europe in May 2021 and the situation in the UK

• Learn how to CE mark a device or to UKCA mark your device

• Learn how to classify medical devices

• Determine the information required for CE marking or UKCA mark

• Understand the role of the Notified Body and the National Competent Authority

• Learn about the clinical evidence that is required to CE/UKCA mark a product and the processes involved


Day 1:

• What is a Medical Device?: How you determine if your product is a medical device; what regulations govern the marketing of medical devices; and how devices are classified

• The CE Marking process: How to get a CE mark for your device; what the process is; what regulations, guidance and standards you need to follow; and what documentation you need. Notified Bodies, National Competent Authorities and Authorized representatives – who they are and what do they do.

• Workshop on Classification

Day 2:

• Clinical evidence for medical devices: What evidence you need; when and how you collect it; and what the regulations and guidance applicable to medical device clinical studies are (including clinical evaluation and clinical investigation).

• Brexit and the UK market for medical devices

• Course Quiz – covering Day 1 and Day 2

The training course will be run by Janette Benaddi, Medipex Associate.

Spaces are limited and registration is essential. Please note in order to ensure all participants get the maximum out of the course by registering you are committing to attending the full duration of the course over both days.

This course will be delivered by the trainer remotely via video conferencing software. Information about how to join the conferencing call will be emailed to everyone that has registered.

Free to staff and postgraduate research students at Translate partner universities (Bradford, Huddersfield, Leeds, Leeds Beckett, Sheffield Hallam and York).

Places for industry and clinical representatives are available at a cost of £45, please email Kelly Broadbent ( to secure your ticket.

The registration process is being managed through Eventbrite, a third-party platform that provides a comprehensive event experience for you and us. This means you are providing data to Eventbrite and must agree to their privacy policy terms, and we will also use your data as per our own privacy policy. If you have any questions get in touch via