What is the webinar about?

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.

Who should attend?

  • Manufacturers (those with UKCA certification and those utilising the CE marking acceptance route to place devices on the GB market
  • Large corporations and SMEs)
  • Medical devices and IVDs
  • Consultants and UK RPs

What will participants gain?

Participants will 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. And an understanding of how to ensure PSUR-compliance for documents covering both the EU & Great Britain regulations.

Speakers

Jenifer 
Hannon
PMS Regulatory Lead
Vishal
Thakker
Head of UK Approved Body
 

To find out more about Medical Devices visit our dedicated Medical Devices webpage and follow us on LinkedIn at BSI Medical Devices.

Email: us.medicaldevices@bsigroup.com

Phone: +1 800 862 4977

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