UK Conformity Assessed (UKCA) Marking for Medical Devices
Since 1 January 2021, there have been a number of changes to how medical devices are placed on the market in the UK. With a substantial reform of the current UK regulatory framework for medical devices in July 2025, the challenges facing medical device companies, regulators and conformity assessment bodies are growing. The requirements for this new UKCA mark will impact technical documentation, labelling, logistics and regulatory compliance.
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Benefits of attending
- Understand the requirements to achieve UKCA
- Know the differences between UKCA and CE marking
- Learn how to align your conformity assessment procedures to meet UKCA and CE marking requirements
- Consider the requirements for the Northern Ireland market
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International Professional & Industry Academy (IPI) is an international leading professional training organisation based in London. Our training solutions provide a return on your investment with measurable results, and are delivered by experienced professionals and managed with exceptional care and...
I was hoping to get more information on how to get an UKCA marking from a Medical Affairs point of view. I accomplished this.