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Question HL856: tabled on 8 June 2021 and due for answer by 22 June 2021

This type of business sits within the Questions & Statements category.

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Question text

To ask Her Majesty's Government what plans they have to follow the approach of the government of the United States' Food and Drug Administration in adapting regulatory requirements by putting clinical evidence into the post-market approval phase and improving the introduction of medical innovation devices.
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Item that is new or altered.
[I] Indicates that the member concerned has a relevant registered interest.
* Item is an oral question.
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