Join us for our PMS in Great Britain webinar on 25 March 2025
This insightful webinar will introduce the PMS requirements under the new regulations in Great Britain for Post-market Surveillance. Our speakers will provide an overview of the similarities and key deviations the UK PMS regulation has from EU MDR/IVDR. In addition, an update/ a look to the future of changes anticipated to UK MDR core regulations will be discussed.
What will participants gain?
An understanding of how the new regulation will impact any manufacturer placing medical devices on the market in or putting into service in Great Britain.
An understanding of how to ensure PSUR-compliance for documents covering both the EU & Great Britain regulations.
Who should attend?
This BSI webinar is designed for manufacturers, specifically those with UKCA certification and those utilising the CE marking acceptance route to place devices on the GB market. The webinar will be beneficial to large corporations and SMEs, medical devices and IVDs, consultants, and UK RPs.
