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Cover: 9780117081079 | Medicines and Healthcare products Regulatory Agency: Good cl | Agency
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Medicines and Healthcare products Regulatory Agency: Good cl
Taschenbuch von Medicines and Healthcare products Regulatory Agency
Sprache: Englisch

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Beschreibung
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
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
Details
Erscheinungsjahr: 2012
Medium: Taschenbuch
Seiten: 564
Inhalt: Kartoniert / Broschiert
ISBN-13: 9780117081079
ISBN-10: 0117081078
Sprache: Englisch
Einband: Kartoniert / Broschiert
Autor: Medicines and Healthcare products Regulatory Agency
Redaktion: Medicines and Healthcare Products Regula
Hersteller: TSO
Abbildungen: figs, tables
Maße: 246 x 174 x 27 mm
Von/Mit: Medicines and Healthcare products Regulatory Agency
Erscheinungsdatum: 24.09.2012
Gewicht: 1,236 kg
preigu-id: 126731401
Details
Erscheinungsjahr: 2012
Medium: Taschenbuch
Seiten: 564
Inhalt: Kartoniert / Broschiert
ISBN-13: 9780117081079
ISBN-10: 0117081078
Sprache: Englisch
Einband: Kartoniert / Broschiert
Autor: Medicines and Healthcare products Regulatory Agency
Redaktion: Medicines and Healthcare Products Regula
Hersteller: TSO
Abbildungen: figs, tables
Maße: 246 x 174 x 27 mm
Von/Mit: Medicines and Healthcare products Regulatory Agency
Erscheinungsdatum: 24.09.2012
Gewicht: 1,236 kg
preigu-id: 126731401
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