Published 13 January 2010, doi:10.1136/bmj.c134
Cite this as: BMJ 2010;340:c134

Letters

The truth about Tamiflu?

Data access is matter of trust

The first 100% of the full text of this article appears below.

The UK Faculty of Public Health strongly supports the BMJ’s 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


Competing interests: None declared.

  1. Godlee F. We want raw data, now. BMJ 2009;339:b5405. (10 December.)[Free Full Text]

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Relevant Article

We want raw data, now
Fiona Godlee
BMJ 2009 339: b5405. [Extract] [Full Text]




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