logo

EbookBell.com

Most ebook files are in PDF format, so you can easily read them using various software such as Foxit Reader or directly on the Google Chrome browser.
Some ebook files are released by publishers in other formats such as .awz, .mobi, .epub, .fb2, etc. You may need to install specific software to read these formats on mobile/PC, such as Calibre.

Please read the tutorial at this link:  https://ebookbell.com/faq 


We offer FREE conversion to the popular formats you request; however, this may take some time. Therefore, right after payment, please email us, and we will try to provide the service as quickly as possible.


For some exceptional file formats or broken links (if any), please refrain from opening any disputes. Instead, email us first, and we will try to assist within a maximum of 6 hours.

EbookBell Team

Supply Chain Management In The Drug Industry Delivering Patient Value For Pharmaceuticals And Biologics 1st Edition Hedley Rees

  • SKU: BELL-2367984
Supply Chain Management In The Drug Industry Delivering Patient Value For Pharmaceuticals And Biologics 1st Edition Hedley Rees
$ 31.00 $ 45.00 (-31%)

4.0

96 reviews

Supply Chain Management In The Drug Industry Delivering Patient Value For Pharmaceuticals And Biologics 1st Edition Hedley Rees instant download after payment.

Publisher: Wiley
File Extension: PDF
File size: 4.63 MB
Pages: 440
Author: Hedley Rees
ISBN: 9780470555170, 0470555173
Language: English
Year: 2011
Edition: 1

Product desciption

Supply Chain Management In The Drug Industry Delivering Patient Value For Pharmaceuticals And Biologics 1st Edition Hedley Rees by Hedley Rees 9780470555170, 0470555173 instant download after payment.

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.

Related Products