Published 14 April 2009, doi:10.1136/bmj.b1499
Cite this as: BMJ 2009;338:b1499

Letters

Sharing medical research data

Whose rights and who’s right?

The first 150 words of the full text of this article appear below.

The moral tone of Groves’ editorial—research is publicly funded; fellow scientists and citizens have a "right" to access "raw numbers, analyses, facts, ideas, and images"; some naughty researchers are colluding with industry to "keep the data hidden away"—was inappropriate.1

Firstly, an increasing number of journal editors are making naive assumptions about the nature of research knowledge. A proportion of such knowledge—for example, in basic sciences—can legitimately be treated as "facts" or "raw numbers" that can be extracted from their context and analysed unproblematically by others at some future date. But the data behind most BMJ papers (broadly, health services research) is not so cleanly cleaved from the context in which it was collected or the people who supplied it and interpreted it. There is an important literature on the lack of transferability of knowledge between communities even in the basic sciences.2 3 The problem increases as the unit of analysis moves . . . [Full text of this article]

Trisha Greenhalgh, professor of primary health care1

1 University College London

p.greenhalgh@ucl.ac.uk


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