Proceeding contribution from Julia Goldsworthy (Liberal Democrat) in the House of Commons on Thursday, 8 December 2005. It occurred during Estimates day on Department of Health.
Department of Health
It is of course important to make such drugs available as quickly as possible, but certain systemic problems have been highlighted, such as ““NICE blight””. We need to take steps to prevent such exceptions from having to be made. Finally, given moves to increase the transparency of data relating to clinical trials, why do negotiations with the Treasury on the pharmaceutical price regulation scheme take place in such deep secrecy? Do the Department plan to make this process more open? I turn finally to other potential dangers and difficulties for patients—
Secondary information
- Type
- Proceeding contribution
- Reference
- 440 c1033
- Session
- 2005-06
- Chamber / Committee
- House of Commons chamber
- Subjects
- Advertising Licensing Expenditure Drugs Government departments Industry Prescription drugs Department of Health Medicines and Healthcare products Regulatory Agency Research Regulation Safety National Institute for Health and Care Excellence Registration Clinical trials
- Link
- View this Proceeding contribution on www.publications.parliament.uk
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- 2025-11-24 15:50:32 +0000
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