Good Design Practices for GMP Pharmaceutical Facilities (Drugs and the Pharmaceutical Sciences)

Read * Good Design Practices for GMP Pharmaceutical Facilities (Drugs and the Pharmaceutical Sciences) by Brand: CRC Press ↠ eBook or Kindle ePUB. Good Design Practices for GMP Pharmaceutical Facilities (Drugs and the Pharmaceutical Sciences) A convenient single-source reference for anyone involved in the planning, construction, validation, and maintenance of modern pharmaceutical facilities, this guide assists project managers as they develop, diagram, and implement pharmaceutical production facility projects-demonstrating how advances in technology and external regulation can impact the production and efficacy of a pharmaceutical facility and the products it produces.]

Good Design Practices for GMP Pharmaceutical Facilities (Drugs and the Pharmaceutical Sciences)

Author :
Rating : 4.24 (964 Votes)
Asin : 0824754638
Format Type : paperback
Number of Pages : 576 Pages
Publish Date : 2015-04-18
Language : English

DESCRIPTION:

Useful, but not worth the money I had to buy this book for a class. It was very helpful in understanding the GMP requirements for facilities - drug, biologic, API, etc. It had logical and useful information.The pictures and graphs used were good as well.However, the wording was horiffic. I noticed three or four spelling/grammar errors each chapter. Some sentences did not make any sense, and confused me even more!If they are going to charge $160 a book, they should have had a proofreader look at the finished product.

"immensely informative, rich in detail, and well-indexed.a useful addition to the company library." -Organic Process Research and Development

A convenient single-source reference for anyone involved in the planning, construction, validation, and maintenance of modern pharmaceutical facilities, this guide assists project managers as they develop, diagram, and implement pharmaceutical production facility projects-demonstrating how advances in technology and external regulation can impact the production and efficacy of a pharmaceutical facility and the products it produces.

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