Supply Chain Management in the Drug Industry 在线电子书 pdf 下载 txt下载 epub 下载 mobi 下载 2024


Supply Chain Management in the Drug Industry

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Rees 作者
John Wiley & Sons
译者
2011-1-14 出版日期
456 页数
GBP 92.95 价格
Hardcover
丛书系列
9780470555170 图书编码

Supply Chain Management in the Drug Industry 在线电子书 图书标签: 供应链  药品政策  医药   


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Supply Chain Management in the Drug Industry 在线电子书 epub 下载 mobi 下载 pdf 下载 txt 下载 2024

Supply Chain Management in the Drug Industry 在线电子书 epub 下载 mobi 下载 pdf 下载 txt 下载 2024

Supply Chain Management in the Drug Industry 在线电子书 pdf 下载 txt下载 epub 下载 mobi 下载 2024



Supply Chain Management in the Drug Industry 在线电子书 用户评价

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2012-01-29读毕,将供应链管理的各种相关知识以隐喻、经验的形式串连在一起,可以作为药品供应链管理的入门书来读。部分章节技术性很强,不是和很好读

评分

2012-01-29读毕,将供应链管理的各种相关知识以隐喻、经验的形式串连在一起,可以作为药品供应链管理的入门书来读。部分章节技术性很强,不是和很好读

评分

2012-01-29读毕,将供应链管理的各种相关知识以隐喻、经验的形式串连在一起,可以作为药品供应链管理的入门书来读。部分章节技术性很强,不是和很好读

评分

2012-01-29读毕,将供应链管理的各种相关知识以隐喻、经验的形式串连在一起,可以作为药品供应链管理的入门书来读。部分章节技术性很强,不是和很好读

评分

2012-01-29读毕,将供应链管理的各种相关知识以隐喻、经验的形式串连在一起,可以作为药品供应链管理的入门书来读。部分章节技术性很强,不是和很好读

Supply Chain Management in the Drug Industry 在线电子书 著者简介

Hedley Rees runs the independent consulting company Biotech PharmaFlow, which specializes in pharmaceutical supply chain management. He has been actively building, managing, and continuously improving supply chains in biotech for the last fifteen years.


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Supply Chain Management in the Drug Industry 在线电子书 pdf 下载 txt下载 epub 下载 mobi 在线电子书下载

Supply Chain Management in the Drug Industry 在线电子书 图书描述

This book bridges the gap between practitioners of supply-chain management and pharmaceutical industry experts. It aims to help both these groups understand the different worlds they live in and how to jointly contribute to meaningful improvements in supply-chains within the globally important pharmaceutical sector. Scientific and technical staff must work closely with supply-chain practitioners and other relevant parties to help secure responsive, cost effective and risk mitigated supply chains to compete on a world stage. This should not wait until a drug has been registered, but should start as early as possible in the development process and before registration or clinical trials. The author suggests that CMC (chemistry manufacturing controls) drug development must reset the line of sight – from supply of drug to the clinic and gaining a registration, to the building of a patient value stream. Capable processes and suppliers, streamlined logistics, flexible plant and equipment, shorter cycle times, effective flow of information and reduced waste. All these factors can and should be addressed at the CMC development stage.

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