Abstract
Background: In their paper "Research approvals iceberg: how a 'low-key' study in England needed 89 professionals to approve it and how we can do better" Petrova and Barclay highlight concerns with the health research regulatory environment in the UK.
Discussion: As long-standing chairs of NHS research ethics committees, researchers, and also academics in research ethics, we are also often frustrated with the regulatory process in the UK. However, we think that Petrova and Barclay's analysis is misleading because it conflates research ethics with governance and funding processes, thus failing to adequately distinguish between the national coordinating function of the Health Research Authority, local research governance processes, and interactions with research sponsors and/or the Clinical Research Network.
| Original language | English |
|---|---|
| Article number | 100 |
| Number of pages | 4 |
| Journal | BMC Medical Ethics |
| Volume | 20 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 24 Dec 2019 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 16 Peace, Justice and Strong Institutions
Keywords
- research ethics
- governance
- trials
- ethics committee
- REC
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Registration audit of clinical trials given a favourable opinion by UK research ethics committees
Denneny, C., Bourne, S. & Kolstoe, S. E., 21 Feb 2019, In: BMJ Open. 9, 2, e026840.Research output: Contribution to journal › Article › peer-review
Open AccessFile317 Downloads (Pure)
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