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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