L

Lord Kamall (Con)

Speaking in the House of Lords on 28 November 2024

Debate

Medical Devices (Post-market Surveillance Requirements) (Amendment) (Great Britain) Regulations 2024

Contribution

I would like to have some more details, in writing, about the conversations that we will have with the EU if our post-market surveillance finds something wrong with a product that has a CE mark to make sure that that will be done co-operatively and will not be seen as causing unnecessary friction. I know that the Minister discussed international co-operation in an earlier answer. There is no need to answer now, but if he could include that in a letter to me that would be welcome.

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