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Author : James I. Wells
Publisher : CRC Press
Page : 232 pages
File Size : 51,9 Mb
Release : 1993-09-30
Category : Medical
ISBN : 013662958X
Dealing exclusively with compression technology, this text reflects the continued popularity of the tablet as a drug form, and thereby the need to refine and enhance the pharmaceutical industry's knowledge of compression.
Author : Anonim
Publisher : Unknown
Page : 216 pages
File Size : 46,6 Mb
Release : 1993
Category : Electronic
ISBN : OCLC:1113047154
Author : Anonim
Publisher : Unknown
Page : 128 pages
File Size : 54,9 Mb
Release : 1987
Category : Electronic
ISBN : OCLC:632872632
Author : M. Rubinstein
Publisher : Unknown
Page : 488 pages
File Size : 43,7 Mb
Release : 2001-01-01
Category : Electronic
ISBN : 0136628346
Author : James Swarbrick
Publisher : CRC Press
Page : 880 pages
File Size : 46,9 Mb
Release : 2013-07-01
Category : Medical
ISBN : 9781439808238
Presenting authoritative and engaging articles on all aspects of drug development, dosage, manufacturing, and regulation, this Third Edition enables the pharmaceutical specialist and novice alike to keep abreast of developments in this rapidly evolving and highly competitive field. A dependable reference tool and constant companion for years to com
Author : M. Rubinstein
Publisher : Unknown
Page : 200 pages
File Size : 52,8 Mb
Release : 1991-06-30
Category : Electronic
ISBN : 0745803423
Several different aspects of instrumentation are covered in this book which evaluates compression processes and the mechanisms of consolidation and compares methods used by workers currently researching in the field. A large portion explores current knowledge in powder consolidation from instrumentation and powder compaction view-points.
Author : Perry Albert Foote
Publisher : Unknown
Page : 256 pages
File Size : 49,9 Mb
Release : 1926
Category : Tablets (Medicine)
ISBN : WISC:89085936011
Author : Reynir Eyjolfsson
Publisher : Academic Press
Page : 68 pages
File Size : 49,6 Mb
Release : 2014-10-15
Category : Medical
ISBN : 9780128021873
Design and Manufacture of Pharmaceutical Tablets offers real world solutions and outcomes of formulation and processing challenges of pharmaceutical tablets. This book includes numerous practical examples related to actual formulations that have been validated and marketed and covers important data in the areas of stability, dissolution, bioavailibity and processing. It provides important background and theoretical information on design and manufacturing and includes a full section dedicated to design experimental methodology and statistics. In addition, this book offers a a general discussion of excipients used in proper tablet design along with practical examples related to excipients. Drug development scientists in industry and academia, as well as students in the pharmaceutical sciences will greatly benefit from the practical knowledge and case examples provided throughout this book. Incorporates important mathematical models and computational applications Includes unique content on central composite design and augmented simplex lattice Provides background on important design principles with emphasis on quality-based design (QBD) of pharmaceutical dosage forms
Author : NIIR Board
Publisher : ASIA PACIFIC BUSINESS PRESS Inc.
Page : 636 pages
File Size : 53,7 Mb
Release : 2004-01-01
Category : Electronic
ISBN : 9788178330549
Drugs and pharmaceutical industry plays a vital role in the economic development of a nation. It is one of the largest and most advanced sectors in the world, acting as a source for various drugs, medicines and their intermediates as well as other pharmaceutical formulations. India has come a long way in this field, from a country importing more than 95% of its requirement of drugs and pharmaceuticals; India now is exporting it even to developed countries. Being the intense knowledge driven industry, it offers innumerable business opportunities for the investors/ corporate the world over. The existence of well defined and strong pharmaceutical industry is important for promoting and sustaining research and developmental efforts and initiatives in an economy as well as making available the quality medicines to all at affordable prices. That is, it is essential to improve the health status of the individuals as well as the society as a whole, so that positive contributions could be made to the economic growth and regional development of a country. On the global platform, India holds fourth position in terms of volume and thirteenth position in terms of value of production in pharmaceuticals. The pharmaceutical industry has been producing bulk drugs belonging to all major therapeutic groups requiring complicated manufacturing processes as well as a wide range of pharmaceutical machinery and equipments. The modern Indian Pharmaceutical Industry is recent and its foundation was laid in the beginning of the current century. The pharmaceutical industry can be broadly categorised as bulk drugs, formulations, IV fluids and pharmaceutical aids (such as medical equipment, hospital disposables, capsules, etc.). Special feature of the pharmaceutical industry is a large number of manufacturers in the small scale sector. The government is also encouraging the SSI sector providing some incentives. The recent developments in the technology and R & D work in this field have led to the increased growth rate of industries and have established Indian Pharmaceutical industries in the international market. The content of the book includes information about properties, general methods of analysis, methods of manufacture, of different types of drugs and pharmaceuticals. Some of the fundamentals of the book are polymeric materials used in drug delivery systems , theoretical aspects of friction and lubrication , a convenient method for conversion of quinine to quinidine, formulation and evaluation of bio-available enteric-coated erythromycin and metronidazole tablets, extraction of virginiamycin, antipyretics and analgesics, column chromatographic assay of aspirin tablets, differentiating titration of phenacetin and caffeine, infrared spectra of some compounds of pharmaceutical interest etc. This book covers an intensive study on manufacturing, production, formulation and quality control of drugs and pharmaceuticals with technology involved in it. This book is an invaluable resource for technologists, professionals and those who want to venture in this field.
Author : S. Bharath
Publisher : Pearson Education India
Page : 345 pages
File Size : 53,8 Mb
Release : 2013
Category : Electronic
ISBN : 9789332520240
Pharmaceutical Technology – Concepts and Applications articulates on the various pharmaco-technological concepts associated with industrial pharmacy. The book not only focuses on providing comprehensive information on formulation development and affiliated areas but also emphasizes on their industrial applications. With a plethora of examples that illustrate important concepts, the book equips students of pharmacy to rise to the requirements of the industry.
Author : Peter Ridgway Watt
Publisher : Ellis Horwood
Page : 446 pages
File Size : 50,9 Mb
Release : 1988-01-01
Category : Comprimés
ISBN : 0745805205
Author : James Swarbrick,James C. Boylan
Publisher : CRC Press
Page : 342 pages
File Size : 43,8 Mb
Release : 2000-12-05
Category : Medical
ISBN : 082472819X
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!
Author : Dilip M. Parikh
Publisher : CRC Press
Page : 532 pages
File Size : 44,8 Mb
Release : 1997-06-17
Category : Medical
ISBN : 0824798821
Integrating the basic principles and industrial practices of pharmaceutical granulation production, this book discusses technologies and demonstrates cost-effective approaches to manufacturing solid-dosage forms with content uniformity and consistent physical properties while complying with regulatory requirements. Specialists from pharmaceutical companies, academia, and the U.S. Drug Regulatory Affairs agency address current and changing practices in industrial drug granulation production. Text, charts, figures, and photographs illustrate the pros and cons of diverse methods and technologies for accurately achieving strong bonding of particles in tablets and capsules.
Author : Anonim
Publisher : Unknown
Page : 128 pages
File Size : 46,9 Mb
Release : 1988
Category : Pharmaceutical chemistry
ISBN : LCCN:88025664
Covers the discovery development,regulation, manufacturing, and commercialization of drugs and dosage forms. Includes pharmaceuticals,pharmacokinetics, analytical chemistry, quality assurance, toxicology and the manufacturing process.
Author : Fernando Muzzio,Sarang Oka
Publisher : Elsevier
Page : 442 pages
File Size : 46,6 Mb
Release : 2022-04
Category : Medical
ISBN : 9780128134795
How to Design and Implement Powder-to-Tablet Continuous Manufacturing Systems provides a comprehensive overview on the considerations necessary for the design of continuous pharmaceutical manufacturing processes. The book covers both the theory and design of continuous processing of associated unit operations, along with their characterization and control. In addition, it discusses practical insights and strategies that the editor and chapter authors have learned. Chapters cover Process Analytical Technology (PAT) tools and the application of PAT data to enable distributed process control. With numerous case studies throughout, this valuable guide is ideal for those engaged in, or learning about, continuous processing in pharmaceutical manufacturing. Discusses the development of strategy blueprints in the design of continuous processes Shows how to create process flowsheet models from individual unit operation models Includes a chapter on characterization methods for materials, the use of statistical methods to analyze material property data, and the use of material databases Covers the evolving regulatory expectations for continuous manufacturing Provides readers with ways to more effectively navigate these expectations
