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pharmaceutical technology quality control matches 16 work(s)
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Product Description: This revised publication serves as a handy and current reference for professionals engaged in planning, designing, building, validating and maintaining modern cGMP pharmaceutical manufacturing facilities in the U.S. and internationally...read more
Hardcover:
9781482258905 | 2 revised edition (CRC Pr I Llc, August 17, 2016), cover price $179.95 | About this edition: This revised publication serves as a handy and current reference for professionals engaged in planning, designing, building, validating and maintaining modern cGMP pharmaceutical manufacturing facilities in the U.
9780824754631 | CRC Pr I Llc, June 7, 2005, cover price $199.95 | About this edition: 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.
9780849398537 | CRC Pr I Llc, March 25, 2005, cover price $55.01
Hardcover:
9781493923151 | Springer Verlag, April 2, 2015, cover price $279.00
Paperback:
9780395700945, titled "Insight Pocket Guides New York City" | 2nd edition (Apa Productions, March 1, 1995), cover price $12.95 | also contains Insight Pocket Guides New York City
Hardcover:
9780849370557 | 3 edition (CRC Pr I Llc, September 25, 2007), cover price $209.95
Product Description: Spanning every critical element of validation for any pharmaceutical, diagnostic, medical device or equipment, and biotech product, this Second Edition guides readers through each step in the correct execution of validating processes required for non-aseptic and aseptic pharmaceutical production...read more
Hardcover:
9780849395291 | 2 har/cdr edition (CRC Pr I Llc, September 30, 2006), cover price $252.00 | About this edition: Spanning every critical element of validation for any pharmaceutical, diagnostic, medical device or equipment, and biotech product, this Second Edition guides readers through each step in the correct execution of validating processes required for non-aseptic and aseptic pharmaceutical production.
Product Description: Often considered a necessary evil by the pharmaceutical industry, validation is still understood by many as unrestrained bureaucracy, paperwork, and procedures whose roots and logic are obscure and only serve to slow down progress...read more (view table of contents, read Amazon.com's description)
Hardcover:
9780849323409 | CRC Pr I Llc, March 1, 2004, cover price $157.95 | About this edition: Often considered a necessary evil by the pharmaceutical industry, validation is still understood by many as unrestrained bureaucracy, paperwork, and procedures whose roots and logic are obscure and only serve to slow down progress.
Product Description: Written especially for the pharmaceutical industry professional, this book addresses each part of the life-cycle of engineering change control. It covers issues in the EU and US and describes the operational requirements and responsibilities that ensure change controls are effectively applied and recorded...read more
Hardcover:
9780849320613 | 2 edition (CRC Pr I Llc, December 1, 2003), cover price $157.95 | About this edition: Written especially for the pharmaceutical industry professional, this book addresses each part of the life-cycle of engineering change control.
Product Description: One of the most common reasons so many new drug, medical device, or equipment applications are rejected each year by the FDA is the failure to properly develop and document plans and procedures. This is required of both U.S. and foreign companies wishing to market their products in the United States...read more
Hardcover:
9781574443318 | Hardcover with CD edition (CRC Pr I Llc, January 1, 2002), cover price $259.95 | About this edition: One of the most common reasons so many new drug, medical device, or equipment applications are rejected each year by the FDA is the failure to properly develop and document plans and procedures.
(view table of contents)
Hardcover:
9781574443301 | Hardcover with CD edition (CRC Pr I Llc, January 1, 2002), cover price $199.95
Product Description: Written by an expert for those who must design validatable cleaning processes and then validate those processes, this book discusses interdependent topics from various technical areas and disciplines. It shows how each piece of the cleaning process fits into the validation program, making it more defensible in both internal quality audits and external regulatory audits...read more (view table of contents, read Amazon.com's description)
Hardcover:
9781574911169 | CRC Pr I Llc, January 1, 2000, cover price $209.95 | About this edition: Written by an expert for those who must design validatable cleaning processes and then validate those processes, this book discusses interdependent topics from various technical areas and disciplines.
Product Description: Change control is important for maintaining the quality of the product, the safety of product and operation, the protection of the environment, and the profitability of the company. Beginning with basic preparatory information, this book covers all aspects of change control: planning, checking, procedures, and key aspects of quality control throughout the entire change control process...read more (view table of contents, read Amazon.com's description)
Hardcover:
9781574910964 | CRC Pr I Llc, January 1, 1999, cover price $179.95 | About this edition: Change control is important for maintaining the quality of the product, the safety of product and operation, the protection of the environment, and the profitability of the company.
Hardcover:
9780824793845 | 2 ill edition (CRC Pr I Llc, November 1, 1998), cover price $260.00
Product Description: While FDA regulations, cGMP, GLP, GCP, and the industry standard ISO 9000 require that documentation be established and followed, they do not provide guidelines on how to produce that documentation. Pharmaceutical Equipment Validation gives details on how to demonstrate compliance, what data to use, and how to produce the appropriate documentation...read more
Hardcover:
9781574910797 | CRC Pr I Llc, August 1, 1998, cover price $209.95 | About this edition: While FDA regulations, cGMP, GLP, GCP, and the industry standard ISO 9000 require that documentation be established and followed, they do not provide guidelines on how to produce that documentation.
Product Description: Good Drug Regulatory Practices offers a series of policies and procedures to assure quality and timely regulatory submissions to national regulatory agencies. This book begins with introductory chapters describing the need for policy documentation, and the philosophy underlying the policies, and presents policies and standards that can be used as presented or adapted to individual situations in your company...read more (view table of contents, read Amazon.com's description)
Hardcover:
9781574910513 | Lslf edition (CRC Pr I Llc, October 1, 1997), cover price $188.95 | About this edition: Good Drug Regulatory Practices offers a series of policies and procedures to assure quality and timely regulatory submissions to national regulatory agencies.
Product Description: Interpharm Press Inc, 1997-06.
Hardcover:
9781574910421 | Interpharm Pr, June 1, 1997, cover price $229.00 | About this edition: Interpharm Press Inc, 1997-06.
Product Description: The importance of quality assurance in the production, storage and use of manufactured preparations is widely recognized. This book encapsulates the issues involved in the manufacture of non-steriles, such as creams, ointments, herbal remedies, shampoos, soaps and toiletry products (as opposed to sterile drugs and injectible products)...read more
Hardcover:
9780748404377, titled "Microbial Quality Assurance in Pharmaceuticals, Cosmetics, and Toiletries" | 2 edition (CRC Pr I Llc, May 1, 1996), cover price $253.00 | About this edition: The importance of quality assurance in the production, storage and use of manufactured preparations is widely recognized.
Product Description: Book by Denyer, S.P.
Hardcover:
9780133728224 | Ellis Horwood Ltd, January 1, 1991, cover price $170.00 | About this edition: Book by Denyer, S.
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