Review of new regulations for the conduct of clinical trials of investigational medicinal products

Bollapragada, S., Norrie, J. and Norman, J. (2007) Review of new regulations for the conduct of clinical trials of investigational medicinal products. BJOG: An International Journal of Obstetrics and Gynaecology, 114(8), pp. 917-921. (doi: 10.1111/j.1471-0528.2007.01415.x)

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Abstract

The EU Clinical Trials Directive came into force on 1 May 2004 and has changed the face of Clinical Trials of investigational medicinal products in the UK. An enthusiastic registrar or consultant who comes up with an idea for a therapeutic intervention now needs to comply with a complex and demanding set of legal, ethical and regulatory requirements, contravention of which may lead to criminal proceedings. The aim of this review was to detail the relevant procedures and regulations and to provide a 'user-friendly' guide to obstetricians and gynaecologists wishing to conduct a clinical trial of an investigational medicinal product. Sources of further information are listed.

Item Type:Articles
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Norrie, Prof John and Norman, Professor Jane
Authors: Bollapragada, S., Norrie, J., and Norman, J.
College/School:College of Medical Veterinary and Life Sciences > School of Health & Wellbeing > Robertson Centre
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Journal Name:BJOG: An International Journal of Obstetrics and Gynaecology
Publisher:Wiley-Blackwell Publishing Ltd.
ISSN:1470-0328
ISSN (Online):1471-0528

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