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Published 13 January 2010, doi:10.1136/bmj.c134
Cite this as: BMJ 2010;340:c134
| The first 100% of the full text of this article appears below. |
The UK Faculty of Public Health strongly supports the BMJs call for mandatory disclosure of raw data of all trials cited in drug licensing applications and marketing claims.1
We see this as a first step towards a position in which only external independent trials published in peer reviewed journals, with full access to raw data, should be allowable when seeking a licence or marketing a product. This would require international agreement by health technology regulators.
Interpreting the evidence base for healthcare planning and commissioning is a key public health function. Full disclosure and openness to scrutiny of evidence on efficacy and safety are crucial if the pharmaceutical industry is to maintain the full trust and confidence of patients, practitioners, policy makers, and the wider public.
Cite this as: BMJ 2010;340:c134
Alan R Maryon-Davis, president1
1 UK Faculty of Public Health, London NW1 4LB
president@fph.org.uk