Heading: |
Cancer: Medical Treatments |
Question ID: |
1805300 |
UIN: |
HL7769 |
House: |
Lords |
Date tabled: |
2025-05-21 |
Asking Member ID: |
4948 |
Asking Member display name: |
Lord Markham
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Asking Member handle: |
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Asking Member Twitter reference: |
Lord Markham
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Member interest: |
false |
Question text: |
To ask His Majesty's Government what steps they are taking to measure the effectiveness of and potential to rapidly adopt cancer therapies that require non-genomic biomarker testing. |
Is named day: |
false |
Date of holding answer: |
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Date answered: |
2025-06-09 |
Date answer corrected: |
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Is holding answer: |
false |
Is correcting answer: |
false |
Answering Member ID: |
347 |
Answering Member display name: |
Baroness Merron
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Answering Member handle: |
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Answering Member Twitter reference: |
Baroness Merron
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Correcting Member ID: |
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Correcting Member display name: |
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Correcting Member handle: |
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Correcting Member Twitter reference: |
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Answer text: |
The Medicines and Healthcare products Regulatory Agency (MHRA) has a key role in assessing the safety and efficacy of any medicine, and newly licensed medicines are appraised by the National Institute for Health and Care Excellence (NICE).The NICE routine... |
Original answer text: |
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Comparable answer text: |
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Answering body ID: |
17 |
Answering body name: |
Department of Health and Social Care |
Tweeted: |
true |