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This course will provide participants with an overview of the critical changes in relation to EU Medical Device Regulation, along with the implementation timescales.
Description :
The course contains the following elements:
- An overview of new regulation
- The key changes you need to be aware of
- What EU MDR means in practice
- Where you can find further information
- A quiz to test your knowledge
Our core services can be divided into four categories:
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Year Company Registered | - | Export Percentage | - |
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