Download or read book Unit Processes in Pharmacy written by David Ganderton and published by Elsevier. This book was released on 2014-05-20 with total page 259 pages. Available in PDF, EPUB and Kindle. Book excerpt: Pharmaceutical Monographs, Volume 7: Unit Processes in Pharmacy provides a survey of the industrial processes used in the large-scale preparation of pharmaceuticals. This book examines the movement of fluids, the transfer of heat, mass transfer, and the properties of powers. Organized into two parts encompassing 14 chapters, this book begins with an overview of the analysis of the flow of fluids through a permeable bed of solids that is widely applied in filtration, leaching, and several other processes. This text then examines the transfer of heat from one fluid to another across a solid boundary. Other chapters consider the movement of relatively large units of gas, called eddies, from one region to another that causes mixing of the components of the gas. This book discusses as well the principle of filtration. The final chapter deals with the scale of segregation and the intensity of segregation. This book is a valuable resource for undergraduate students of pharmacy and allied subjects.
Download or read book Predictive Modeling of Pharmaceutical Unit Operations written by Preetanshu Pandey and published by Woodhead Publishing. This book was released on 2016-09-26 with total page 465 pages. Available in PDF, EPUB and Kindle. Book excerpt: The use of modeling and simulation tools is rapidly gaining prominence in the pharmaceutical industry covering a wide range of applications. This book focuses on modeling and simulation tools as they pertain to drug product manufacturing processes, although similar principles and tools may apply to many other areas. Modeling tools can improve fundamental process understanding and provide valuable insights into the manufacturing processes, which can result in significant process improvements and cost savings. With FDA mandating the use of Quality by Design (QbD) principles during manufacturing, reliable modeling techniques can help to alleviate the costs associated with such efforts, and be used to create in silico formulation and process design space. This book is geared toward detailing modeling techniques that are utilized for the various unit operations during drug product manufacturing. By way of examples that include case studies, various modeling principles are explained for the nonexpert end users. A discussion on the role of modeling in quality risk management for manufacturing and application of modeling for continuous manufacturing and biologics is also included. Explains the commonly used modeling and simulation tools Details the modeling of various unit operations commonly utilized in solid dosage drug product manufacturing Practical examples of the application of modeling tools through case studies Discussion of modeling techniques used for a risk-based approach to regulatory filings Explores the usage of modeling in upcoming areas such as continuous manufacturing and biologics manufacturingBullet points
Download or read book Pharmaceutical Engineering written by K Sambamurthy and published by New Age International. This book was released on 2007 with total page 504 pages. Available in PDF, EPUB and Kindle. Book excerpt: It Is Well Known That The Applications Of Unit Operations Like Heat Transfer, Evaporation, Extraction, Mixing, Filtration And A Host Of Others Are Quite Common In The Pharmaceutical Industry, Be It In The Production Of Synthetic Drugs, Biological And Microbiological Products Or In The Manufacture Of Pharmaceutical Formulations. As Such Anyone Who Is To Look After These Manufacturing Operations Must Be Quite Knowledgeable With The Theoretical And Equipment Aspects Involved In The Relevant Unit Operations.Since A Major Involvement Of The Pharmacy Graduates Lies In The Numerous Manufacturing Operations Mentioned Above, It Is Very Much Necessary That The Subject Is Taught With A Pharmacy Orientation. There Is No Book So Far Which Has Achieved This. The Existing Books On Unit Operations Give Extensive Theory And Also Deal With A Lot Of Equipment Not Employed In The Pharmaceutical Industry. Due To A Lack Of A Pharmacy-Oriented Book In This Area, The Students And The Teachers Are Facing Difficulties In Many Ways.The Present Book Is The First One Of Its Kind On Pharmaceutical Engineering. The Special Features Of This Book Are As Follows: It Includes Theoretical And Equipment Aspects Relevant To Thepharmaceutical Industry And That Too To The Extent Needed For Pharmacy Graduates And Examples From Pharmaceutical Industry Are Quoted Extensively; Solutions To A Number Of Simpler Numerical Problems Are Given. At The End Of Each Chapter, A Large Number Of Questions, Both Theoretical And Numerical, Are Given. There Is Therefore No Doubt That The Book Will Be Of Great Use Not Only To The Students But Also To The Teachers In The Subject In India And Abroad As Well.
Download or read book Unit Operations in Pharmaceutical Engineering written by Y. Sultana and published by CBS Publishers & Distributors Pvt Limited, India. This book was released on 2018-10-30 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt: Provides comprehensive coverage of theoretical and equipment aspects in unit operations relevant to pharmaceutical industry. All intricate aspects are explained in simple language with specific explanations and substantiated with neat and elaborate diagrammatic sketches.
Download or read book Pharmaceutical Process Engineering written by Anthony J. Hickey and published by CRC Press. This book was released on 2016-03-09 with total page 230 pages. Available in PDF, EPUB and Kindle. Book excerpt: With step-by-step methods of drug production and knowledge of major unit operations and key concepts of pharmaceutical engineering, this guide will help to improve communication among the varied professionals working in the pharmaceutical industry. Key features: REVISION OF A BESTSELLER - Updates include recent advances in the field to keep pharmac
Download or read book Unit processes in pharmacy written by David Ganderton and published by . This book was released on 1968 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Pharmaceutical Engineering written by and published by . This book was released on 2014 with total page 376 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Pharmaceutical Engineering written by and published by . This book was released on 2014 with total page 383 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Pharmaceutical Unit Operations written by Kenneth E. Avis and published by . This book was released on 2001 with total page 348 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Encyclopedia of Pharmaceutical Technology Unit processes in pharmacy the operations to zeta potential written by and published by . This book was released on 1988 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Pharmaceutical Unit Operations written by Kenneth E Avis and published by CRC Press. This book was released on 2019-08-30 with total page 368 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book is a complete, authoritative resource on the coating of tablets, capsules, and other solid dosage forms of therapeutic agents. Fourteen authors cover the industry's technologies. The book begins with a full discussion of the primary processes -- sugar coating, film coating, and microencapsulation -- as well as the rationale for coating, methodologies, formulations, processing methods, and equipment and cleaning. Then it explores automation of the coating process, including hardware and software requirements. Finally, the book examines major stability and quality control issues. Regulations underlie all discussions.
Download or read book Pharmaceutical Engineering and Unit Operations written by David S. Jones and published by Wiley-Blackwell. This book was released on 2014-01-03 with total page 304 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Global Supply Chains in the Pharmaceutical Industry written by Nozari, Hamed and published by IGI Global. This book was released on 2018-11-09 with total page 373 pages. Available in PDF, EPUB and Kindle. Book excerpt: In a rapidly growing global economy, where there is a constant emergence of new business models and dynamic changes to the business ecosystem, there is a need for the integration of traditional, new, and hybrid concepts in the complex structure of supply chain management. Within the fast-paced pharmaceutical industry, product strategy, life cycles, and distribution must maintain the highest level of agility. Therefore, organizations need strong supply chain capabilities to profitably compete in the marketplace. Global Supply Chains in the Pharmaceutical Industry provides innovative insights into the efforts needed to build and maintain a strong supply chain network in order to achieve efficient fulfillment of demand, drive outstanding customer value, enhance organizational responsiveness, and build network resiliency. This publication is designed for supply chain managers, policymakers, researchers, academicians, and students, and covers topics centered on economic cycles, sustainable development, and new forces in the global economy.
Download or read book Process Systems Engineering for Pharmaceutical Manufacturing written by Ravendra Singh and published by Elsevier. This book was released on 2018-03-16 with total page 700 pages. Available in PDF, EPUB and Kindle. Book excerpt: Process Systems Engineering for Pharmaceutical Manufacturing: From Product Design to Enterprise-Wide Decisions, Volume 41, covers the following process systems engineering methods and tools for the modernization of the pharmaceutical industry: computer-aided pharmaceutical product design and pharmaceutical production processes design/synthesis; modeling and simulation of the pharmaceutical processing unit operation, integrated flowsheets and applications for design, analysis, risk assessment, sensitivity analysis, optimization, design space identification and control system design; optimal operation, control and monitoring of pharmaceutical production processes; enterprise-wide optimization and supply chain management for pharmaceutical manufacturing processes. Currently, pharmaceutical companies are going through a paradigm shift, from traditional manufacturing mode to modernized mode, built on cutting edge technology and computer-aided methods and tools. Such shifts can benefit tremendously from the application of methods and tools of process systems engineering. Introduces Process System Engineering (PSE) methods and tools for discovering, developing and deploying greener, safer, cost-effective and efficient pharmaceutical production processes Includes a wide spectrum of case studies where different PSE tools and methods are used to improve various pharmaceutical production processes with distinct final products Examines the future benefits and challenges for applying PSE methods and tools to pharmaceutical manufacturing
Download or read book Continuous Manufacturing of Pharmaceuticals written by Peter Kleinebudde and published by John Wiley & Sons. This book was released on 2017-09-05 with total page 645 pages. Available in PDF, EPUB and Kindle. Book excerpt: A comprehensive look at existing technologies and processes for continuous manufacturing of pharmaceuticals As rising costs outpace new drug development, the pharmaceutical industry has come under intense pressure to improve the efficiency of its manufacturing processes. Continuous process manufacturing provides a proven solution. Among its many benefits are: minimized waste, energy consumption, and raw material use; the accelerated introduction of new drugs; the use of smaller production facilities with lower building and capital costs; the ability to monitor drug quality on a continuous basis; and enhanced process reliability and flexibility. Continuous Manufacturing of Pharmaceuticals prepares professionals to take advantage of that exciting new approach to improving drug manufacturing efficiency. This book covers key aspects of the continuous manufacturing of pharmaceuticals. The first part provides an overview of key chemical engineering principles and the current regulatory environment. The second covers existing technologies for manufacturing both small-molecule-based products and protein/peptide products. The following section is devoted to process analytical tools for continuously operating manufacturing environments. The final two sections treat the integration of several individual parts of processing into fully operating continuous process systems and summarize state-of-art approaches for innovative new manufacturing principles. Brings together the essential know-how for anyone working in drug manufacturing, as well as chemical, food, and pharmaceutical scientists working on continuous processing Covers chemical engineering principles, regulatory aspects, primary and secondary manufacturing, process analytical technology and quality-by-design Contains contributions from researchers in leading pharmaceutical companies, the FDA, and academic institutions Offers an extremely well-informed look at the most promising future approaches to continuous manufacturing of innovative pharmaceutical products Timely, comprehensive, and authoritative, Continuous Manufacturing of Pharmaceuticals is an important professional resource for researchers in industry and academe working in the fields of pharmaceuticals development and manufacturing.
Download or read book Encyclopedia of Pharmaceutical Technology written by James Swarbrick and published by CRC Press. This book was released on 1997-05-23 with total page 504 pages. Available in PDF, EPUB and Kindle. Book excerpt: The Encyclopedia of Pharmaceutical Technology presents authoritative and contemporary articles on all aspects of drug development, dosage forms, manufacturing, and regulation-enabling the specialist and novice alike to keep abreast of developments in this rapidly evolving and highly competitive field. A dependable reference tool and a solid investment for years to come-maintaining currency through its supplements [Volume 18/Supplement 1: Published November, 1998] The Encyclopedia contains interdisciplinary contributions in a wide array of subjects, including Drugs decomposition metabolism pharmaceutical incompatibilities pharmacokinetics physicochemical properties preformulation stability Drug Delivery Systems and Devices-Development and Manufacture analysis and controls bioavailability use of computerization formulation and processing alternatives national and international registration packaging patents process validation scale-up safety and efficacy stability standards Post-Production and Practical Considerations governmental/industrial/professional organizations legal aspects national and international agencies patent life of drugs patient compliance ...and much, much more!
Download or read book How to Develop Robust Solid Oral Dosage Forms written by Bhavishya Mittal and published by Academic Press. This book was released on 2016-10-05 with total page 192 pages. Available in PDF, EPUB and Kindle. Book excerpt: How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval uses a practical and hands-on approach to cover the development process of solid oral dosage forms in one single source. The book details all of the necessary steps from formulation through the post-approval phase and contains industry case studies, real world advice, and troubleshooting tips. By merging the latest scientific information with practical instructions, this book provides pharmaceutical scientists in formulation research and development with a concrete look at the key aspects in the development of solid oral dosage forms. Focuses on important topics, such as robustness, bioavailability, formulation design, continuous processing, stability tests, modified release dosage forms, international guidelines, process scale-up, and much more Part of the Expertise in Pharmaceutical Process Technology series edited by Michael Levin Discusses common, real-world problems and offers both theoretical and practical solutions to these everyday issues
