Published 6 January 2009, doi:10.1136/bmj.a3140
Cite this as: BMJ 2009;338:a3140

Letters

Regulation’s threat to research

Regulation of research

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

In the open season for hunting research ethics committees1 the letters show how researchers may be their own worst enemies. For example, Parker waited for nearly a year for a response from the Medicines and Healthcare Products Regulatory Agency, which need not have been approached.2 He then applied sequentially to the ethics committee and research and development department when he should have done so concurrently at the start. Samuel’s study might have been regarded as audit or service development, not requiring ethical approval.3

The process of ethical review cries out for simplification and abbreviation. For example, a distinction could be made between interventional research and the plethora of projects arising from undergraduate and postgraduate studies in pursuit of degrees.

The unacknowledged source of frustration is government. The Human Tissue Act 2004, for example, is arguably an over-reaction on the part of government and the chief medical officer (with the complicity . . . [Full text of this article]

David E B Powell, chairman1

1 South East Wales Research Ethics Committee, Peniel, Carmarthen SA32 7HF

david.powell58@btopenworld.com


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