The Good Clinical Practice Guide is a brand new publication
covering the legislation, guidance and good practice that relates
to the conduct of clinical trials of medicinal products for human
use in the UK. Detailed and authoritative, this guide will provide
practical advice about implementing the principles of Good Clinical
Practice within the context of the clinical trial regulatory
framework in the European Union. Written and produced by the MHRA,
this is the only guide on Good Clinical Practice available within
Europe which has been produced by a regulatory agency. This title
is aimed at any individual and/or organisation involved in
conducting clinical trials with medicines in the UK, including both
commercial and non-commercial sponsors and hosts of clinical
trials, as well as contract research organisations, clinical
research consultants and other niche providers. The guide
references European legislation and guidance as well as
international standards, so will also be relevant to organisations
conducting trials across Europe and beyond
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