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
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3 of 3 people found the following review helpful:
2.0 out of 5 stars
Useful, but not worth the money,
By L-Train (NJ) - See all my reviews
This review is from: Good Design Practices for GMP Pharmaceutical Facilities (Drugs and the Pharmaceutical Sciences) (Hardcover)
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.
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Inside This Book
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First Sentence:
The pharmaceutical industry is a major global economic force, which increasingly relies on the safe and efficient production of technically advanced products. Read the first page Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
solid dosage facilities, solid dosage facility, relative pressurization, enhanced surface finish, compendial waters, dosage form facilities, multiple effect stills, sulfite injection, sterile manufacturing facility, sterile manufacturing facilities, microbial retentive filters, hot water sanitization, split butterfly valves, critical utility systems, feed water quality, drug matrices, pharmaceutical water systems, vapor compression stills, pharmaceutical manufacturing facilities, disposable cartridge filters, packaging floor, chemical sanitization, sanitization methods, pharmaceutical manufacturing facility, domestic cold water Key Phrases - Capitalized Phrases (CAPs): (learn more)
United States, Editor's Note, International Code Council, National Fire Protection Association, Baseline Guide, Epoxy Epoxy, New York, New Jersey, International Building Code, Environmental Protection Agency, Clean Air Act, Code of Federal Regulations, Baseline Pharmaceutical Engineering Guide, Disabilities Act, European Union, Puerto Rico, Sterile Drug Products Produced, Clean Water Act, Drug Enforcement Agency, Eli Lilly, Inspections of High Purity Water Systems, National Electrical Code, Access Control Materials, American Conference of Governmental Industrial Hygienists, American National Standards Institute New!
Books on Related Topics | Concordance | Text Stats Browse Sample Pages:
Front Cover | Table of Contents | First Pages | Index | Back Cover | Surprise Me!
The pharmaceutical industry is a major global economic force, which increasingly relies on the safe and efficient production of technically advanced products. Read the first page Key Phrases - Statistically Improbable Phrases (SIPs): (learn more)
solid dosage facilities, solid dosage facility, relative pressurization, enhanced surface finish, compendial waters, dosage form facilities, multiple effect stills, sulfite injection, sterile manufacturing facility, sterile manufacturing facilities, microbial retentive filters, hot water sanitization, split butterfly valves, critical utility systems, feed water quality, drug matrices, pharmaceutical water systems, vapor compression stills, pharmaceutical manufacturing facilities, disposable cartridge filters, packaging floor, chemical sanitization, sanitization methods, pharmaceutical manufacturing facility, domestic cold water Key Phrases - Capitalized Phrases (CAPs): (learn more)
United States, Editor's Note, International Code Council, National Fire Protection Association, Baseline Guide, Epoxy Epoxy, New York, New Jersey, International Building Code, Environmental Protection Agency, Clean Air Act, Code of Federal Regulations, Baseline Pharmaceutical Engineering Guide, Disabilities Act, European Union, Puerto Rico, Sterile Drug Products Produced, Clean Water Act, Drug Enforcement Agency, Eli Lilly, Inspections of High Purity Water Systems, National Electrical Code, Access Control Materials, American Conference of Governmental Industrial Hygienists, American National Standards Institute New!
Books on Related Topics | Concordance | Text Stats Browse Sample Pages:
Front Cover | Table of Contents | First Pages | Index | Back Cover | Surprise Me!
Citations (learn more)
This book cites 100
books:
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- Good Manufacturing Practices for Pharmaceuticals: A Plan for Total Quality Control (Drugs and the Pharmaceutical Sciences Series, Vol 78) by Sidney H. Willig on 4 pages
- New Drug Approval Process, Fourth Edition, Accelerating Global Registrations (Drugs and the Pharmaceutical Sciences) by Richard Guarino on 4 pages
- Modern Pharmaceutics by Gilbert S. Banker on 4 pages
- Pharmaceutical Statistics: Practical and Clinical Applications, Fourth Edition, Revised and Expanded (Drugs and the Pharmaceutical Sciences) by Sanford Bolton in Front Matter (1), Front Matter (2), and Front Matter (3)
- Pharmaceutical Process Validation: An International Third Edition (Drugs and the Pharmaceutical Sciences) by Robert A. Nash in Front Matter (1), Front Matter (2), and Front Matter (3)
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