Product Compliance in the UK
With its departure from the European Union, the UK is phasing out the CE marking. The new UKCA marking (UK Conformity Assessed) is the new marking for products in the United Kingdom and indicates that a product placed on the UK market meets national requirements. Here, too, the underlying principle is product safety for medical devices. The new UKCA marking has been mandatory since January 1, 2023.
Learn who is responsible forthe UKCA marking and how you can successfully implement the requirements in your company.
- Content
- Differences between the UKCA mark and the CE marking
- Overview of the conformity assessment process
- Marking options (CE, UKCA, UKNI)
- Role of the responsible person in Great Britain
- Special case of NorthernIreland
- Your Benefits
- You will learn about the various requirements for the UKCA marking.
- You will become familiar with the approval procedures in the UK.
- Methods
Instructor-led sessions, group exercises,facilitated case studies, practical exercises, individual work, real-world case studies, discussions, live coaching, storytelling.
- Target Audience
- RA Specialists
- QM Specialists
- Medical device developers and manufacturers
- Project managers
- Medical device manufacturers and exporters
