NIHR HRC in Community Healthcare: EU Medical Device Regulations Workshop
Friday 20 June 2025
The NIHR HealthTech Research Centre in Community Healthcare is running an interactive online workshop about EU Medical Device Regulations on Tuesday 8th July 2025.
The objective of this HRC workshop is to learn the first key aspects of the EU Medical Device Regulations: to determine when a product is a medical device, what the risk classification of the device is and what the next steps are.
Professor Jeroen Bergmann from the NIHR HRC in Community Healthcare’s Need-Led Device Development and Regulatory theme is hosting the workshop alongside Dr Rita Hendricusdottir from RegMetrics.
What does the workshop cover?
- Basic grounding in EU Medical Device Regulation (‘EU-MDR’) (note this is not for IVDs)
- Interactive guidance through the MDR classification process
- Key regulatory elements and documentation requirements
- Practical experience using the RegMetrics platform
Who would benefit?
Academic researchers, clinicians, innovators, start-ups, SMEs, research councils, and tech transfer organisations developing medical devices or digital health solutions for EU deployment.
Though UK-based organisations will be prioritised initially, this opportunity is open to all. This could be especially valuable for any organisations in your networks who are navigating the often complex regulatory landscape for medical devices.
For more information and to register for the workshop, please use the link below.