Download or read book Inspection in Tablet Manufacture written by Convention for the Mutual Recognition of Inspections. Séminaire and published by . This book was released on 1981 with total page 40 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Inspection in Tablet Manufacture written by Convention for the Mutual Recognition of Inspections in Respect of the Manufacture of Pharmaceutical Products and published by . This book was released on 1980 with total page 36 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Inspection in Tablet Manufacture written by and published by . This book was released on 1980* with total page 36 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Tableting Specification Manual written by American Pharmacists Association and published by American Pharmacists Association (APhA). This book was released on 2006 with total page 156 pages. Available in PDF, EPUB and Kindle. Book excerpt: This is the most comprehensive guide about the design of and specifications for tablet tooling, the design of tablets, and the appropriate compression forces for various types of tooling. The manual provides detailed explanations and supporting illustrations for inspection and maintenance of tooling. Two troubleshooting charts identify common tablet production problems and their remedies.
Download or read book Design and Manufacture of Pharmaceutical Tablets written by Reynir Eyjolfsson and published by Academic Press. This book was released on 2014-10-09 with total page 68 pages. Available in PDF, EPUB and Kindle. Book excerpt: 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
Download or read book Aulton s Pharmaceutics written by Michael E. Aulton and published by Elsevier Health Sciences. This book was released on 2013 with total page 909 pages. Available in PDF, EPUB and Kindle. Book excerpt: "Pharmaceutics is the art of pharmaceutical preparations. It encompasses design of drugs, their manufacture and the elimination of micro-organisms from the products. This book encompasses all of these areas."--Provided by publisher.
Download or read book Inspection and Measurement in Manufacturing written by William Winchell and published by Society of Manufacturing Engineers. This book was released on 1996 with total page 214 pages. Available in PDF, EPUB and Kindle. Book excerpt: For the experienced manufacturing professional, the book offers a review of inspection and measurement concepts, and some new insights into the subject. For those new to inspection and measurement, the text will help them grasp the technology involved and the methods for effectively planning applications.
Download or read book Tableting Specification Manual written by American Pharmaceutical Association. Tableting Specification Steering Committee and published by American Pharmacists Association (APhA). This book was released on 2003 with total page 144 pages. Available in PDF, EPUB and Kindle. Book excerpt: A guide to the design of and specifications for tablet tooling, the design of tablets, and the appropriate compression forces for various types of tooling. It provides explanations and supporting illustrations for inspection and maintenance of tooling. It can be used as a reference on US manufacturing specifications for tablets and tablet tooling.
Download or read book FDA Inspection Operations Manual written by and published by . This book was released on 1990 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Good Manufacturing Practice in Tablet Manufacture written by Convention for the Mutual Recognition of Inspections in Respect of the Manufacture of Pharmaceutical Products and published by . This book was released on 1978 with total page 158 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Pharmaceutical Manufacturing Handbook written by Shayne Cox Gad and published by John Wiley & Sons. This book was released on 2008-03-21 with total page 1384 pages. Available in PDF, EPUB and Kindle. Book excerpt: This handbook features contributions from a team of expert authors representing the many disciplines within science, engineering, and technology that are involved in pharmaceutical manufacturing. They provide the information and tools you need to design, implement, operate, and troubleshoot a pharmaceutical manufacturing system. The editor, with more than thirty years' experience working with pharmaceutical and biotechnology companies, carefully reviewed all the chapters to ensure that each one is thorough, accurate, and clear.
Download or read book Guideline on General Principles of Process Validation written by and published by . This book was released on 1987 with total page 32 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book The Business of Pharmaceutical Inspection written by Convention for the Mutual Recognition of Inspection in Respect of the Manufacture of Pharmaceutical Products Cambridge, England) and published by . This book was released on 1987 with total page 168 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Pharmaceutical Manufacturing Handbook written by Shayne Cox Gad and published by John Wiley & Sons. This book was released on 2008-03-17 with total page 1396 pages. Available in PDF, EPUB and Kindle. Book excerpt: This handbook features contributions from a team of expert authors representing the many disciplines within science, engineering, and technology that are involved in pharmaceutical manufacturing. They provide the information and tools you need to design, implement, operate, and troubleshoot a pharmaceutical manufacturing system. The editor, with more than thirty years' experience working with pharmaceutical and biotechnology companies, carefully reviewed all the chapters to ensure that each one is thorough, accurate, and clear.
Download or read book FDA Inspection Operations Manual written by United States. Department of Health and Human Services and published by . This book was released on 1983 with total page 172 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Countering the Problem of Falsified and Substandard Drugs written by Institute of Medicine and published by National Academies Press. This book was released on 2013-06-20 with total page 377 pages. Available in PDF, EPUB and Kindle. Book excerpt: The adulteration and fraudulent manufacture of medicines is an old problem, vastly aggravated by modern manufacturing and trade. In the last decade, impotent antimicrobial drugs have compromised the treatment of many deadly diseases in poor countries. More recently, negligent production at a Massachusetts compounding pharmacy sickened hundreds of Americans. While the national drugs regulatory authority (hereafter, the regulatory authority) is responsible for the safety of a country's drug supply, no single country can entirely guarantee this today. The once common use of the term counterfeit to describe any drug that is not what it claims to be is at the heart of the argument. In a narrow, legal sense a counterfeit drug is one that infringes on a registered trademark. The lay meaning is much broader, including any drug made with intentional deceit. Some generic drug companies and civil society groups object to calling bad medicines counterfeit, seeing it as the deliberate conflation of public health and intellectual property concerns. Countering the Problem of Falsified and Substandard Drugs accepts the narrow meaning of counterfeit, and, because the nuances of trademark infringement must be dealt with by courts, case by case, the report does not discuss the problem of counterfeit medicines.
Download or read book Guideline on Sterile Drug Products Produced by Aseptic Processing written by Center for Drugs and Biologics (U.S.) and published by . This book was released on 1987 with total page 48 pages. Available in PDF, EPUB and Kindle. Book excerpt:
