Good Clinical Practice Guide

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9780117081079: Good Clinical Practice Guide

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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1.

Great Britain
Editorial: TSO] 2012-09-24, [London? (2012)
ISBN 10: 0117081078 ISBN 13: 9780117081079
Nuevos paperback Cantidad: 5
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Blackwell's
(Oxford, OX, Reino Unido)
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Descripción TSO] 2012-09-24, [London?, 2012. paperback. Estado de conservación: New. Nº de ref. de la librería 9780117081079

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Medicines And Healthcare Products Regulatory Agency
Editorial: TSO, United Kingdom (2012)
ISBN 10: 0117081078 ISBN 13: 9780117081079
Nuevos Paperback Cantidad: 10
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The Book Depository
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Descripción TSO, United Kingdom, 2012. Paperback. Estado de conservación: New. Language: English . Brand New Book. 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. Nº de ref. de la librería AAZ9780117081079

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ISBN 10: 0117081078 ISBN 13: 9780117081079
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Descripción Estado de conservación: New. Nº de ref. de la librería 18764910-n

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Medicines And Healthcare Products Regulatory Agency
Editorial: TSO, United Kingdom (2012)
ISBN 10: 0117081078 ISBN 13: 9780117081079
Nuevos Paperback Cantidad: 10
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The Book Depository US
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Descripción TSO, United Kingdom, 2012. Paperback. Estado de conservación: New. Language: English . Brand New Book. 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. Nº de ref. de la librería AAZ9780117081079

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Medicines and Healthcare products Regulatory Agency
Editorial: Stationery Office 2012-09-24 (2012)
ISBN 10: 0117081078 ISBN 13: 9780117081079
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Chiron Media
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Descripción Stationery Office 2012-09-24, 2012. Estado de conservación: New. Brand new book, sourced directly from publisher. Dispatch time is 24-48 hours from our warehouse. Book will be sent in robust, secure packaging to ensure it reaches you securely. Nº de ref. de la librería NU-GRD-04906872

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Medicines and Healthcare Products Regulatory Agency
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ISBN 10: 0117081078 ISBN 13: 9780117081079
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Descripción TSO, 2012. Estado de conservación: New. 2012. Paperback. Num Pages: 564 pages, figs, tables. BIC Classification: MJ. Category: (G) General (US: Trade). Dimension: 245 x 173 x 26. Weight in Grams: 1240. . . . . . . Nº de ref. de la librería V9780117081079

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Great Britain: Medicines and Healthcare Products Regulatory Agency
Editorial: TSO
ISBN 10: 0117081078 ISBN 13: 9780117081079
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THE SAINT BOOKSTORE
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Descripción TSO. Paperback. Estado de conservación: new. BRAND NEW, Good Clinical Practice Guide, Great Britain: Medicines and Healthcare Products Regulatory Agency, 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. Nº de ref. de la librería B9780117081079

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Stationery Office (Great Britain)
ISBN 10: 0117081078 ISBN 13: 9780117081079
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Descripción Estado de conservación: New. Bookseller Inventory # ST0117081078. Nº de ref. de la librería ST0117081078

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Medicines and Healthcare Products Regulatory Agency
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ISBN 10: 0117081078 ISBN 13: 9780117081079
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Kennys Bookstore
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Descripción TSO. Estado de conservación: New. 2012. Paperback. Num Pages: 564 pages, figs, tables. BIC Classification: MJ. Category: (G) General (US: Trade). Dimension: 245 x 173 x 26. Weight in Grams: 1240. . . . . . Books ship from the US and Ireland. Nº de ref. de la librería V9780117081079

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Great Britain: Medicines and Healthcare Products Regulatory Agency
Editorial: TSO (2012)
ISBN 10: 0117081078 ISBN 13: 9780117081079
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Books2Anywhere
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Descripción TSO, 2012. PAP. Estado de conservación: New. New Book. Shipped from UK in 4 to 14 days. Established seller since 2000. Nº de ref. de la librería GB-9780117081079

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