Quick Guide to Good Clinical Practice

How to Meet International Quality Standard in Clinical Research

Nonfiction, Health & Well Being, Medical, Reference, Biostatistics, Medical Science, Pharmacology
Cover of the book Quick Guide to Good Clinical Practice by Cemal Cingi, Nuray Bayar Muluk, Springer International Publishing
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Author: Cemal Cingi, Nuray Bayar Muluk ISBN: 9783319443447
Publisher: Springer International Publishing Publication: November 15, 2016
Imprint: Springer Language: English
Author: Cemal Cingi, Nuray Bayar Muluk
ISBN: 9783319443447
Publisher: Springer International Publishing
Publication: November 15, 2016
Imprint: Springer
Language: English

This brand-new book offers a reference guide to understanding and applying the rules for properly conducting clinical trials to meet the international quality standard – Good Clinical Practice – provided by the International Conference on Harmonization (ICH). 

The work offers an updated perspective on the clinical research landscape within the context of the clinical trial regulatory frameworks in Europe and the USA. In addition to providing a historical review and a detailed definition of GPC regulations, it includes step-by-step explanations of all the requirements that researchers should bear in mind when designing and performing new trials. Further topics covered include: ethics of clinical research; the drug development process and evolution of regulations; investigator and sponsor responsibilities; and clinical trial protocols.

Written by clinicians for clinicians, the book represents a valuable read also for researchers, pharmacists and all professionals involved in applications to the ethic committees, whose approval is required for new clinical studies.

View on Amazon View on AbeBooks View on Kobo View on B.Depository View on eBay View on Walmart

This brand-new book offers a reference guide to understanding and applying the rules for properly conducting clinical trials to meet the international quality standard – Good Clinical Practice – provided by the International Conference on Harmonization (ICH). 

The work offers an updated perspective on the clinical research landscape within the context of the clinical trial regulatory frameworks in Europe and the USA. In addition to providing a historical review and a detailed definition of GPC regulations, it includes step-by-step explanations of all the requirements that researchers should bear in mind when designing and performing new trials. Further topics covered include: ethics of clinical research; the drug development process and evolution of regulations; investigator and sponsor responsibilities; and clinical trial protocols.

Written by clinicians for clinicians, the book represents a valuable read also for researchers, pharmacists and all professionals involved in applications to the ethic committees, whose approval is required for new clinical studies.

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