Pharmaceutical Quality Assurance PDF Download
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Author | : Mr. Manohar A. Potdar |
Publisher | : Pragati Books Pvt. Ltd. |
Total Pages | : 424 |
Release | : 2006 |
Genre | : Pharmaceutical industry |
ISBN | : 9788185790596 |
Download Pharmaceutical Quality Assurance Book in PDF, ePub and Kindle
Author | : Minal Ghante |
Publisher | : Springer Nature |
Total Pages | : 525 |
Release | : |
Genre | : |
ISBN | : 9819992710 |
Download Modern Aspects of Pharmaceutical Quality Assurance Book in PDF, ePub and Kindle
Author | : Oliver Schmidt |
Publisher | : CRC Press |
Total Pages | : 392 |
Release | : 2000-04-30 |
Genre | : Medical |
ISBN | : 142002602X |
Download Pharmaceutical Quality Systems Book in PDF, ePub and Kindle
When a pharmaceutical company decides to build a Quality System, it has to face the fact that there aren't any guideline that define exactly how such a system has to be built. With terms such as quality system, quality assurance, and quality management used interchangeably, even defining the system's objectives is a problem. This book provides a pr
Author | : World Health Organization |
Publisher | : World Health Organization |
Total Pages | : 250 |
Release | : 2004 |
Genre | : Business & Economics |
ISBN | : 9789241546195 |
Download Quality Assurance of Pharmaceuticals Book in PDF, ePub and Kindle
Over the years, the World Health Organization's Expert Committee on Specifications for Pharmaceutical Preparations, originally created to prepare The International Pharmacopoeia, has made numerous recommendations relevant to quality assurance and control for national regulatory and control systems and the implementation of international standards, but for the most part they have only been available in the annexes to various technical reports. In this second of two volumes, those annexes providing guidelines related to good manufacturing practices and to inspection of manufacturers and drug distribution channels have been gathered and revised. Annotation : 2004 Book News, Inc., Portland, OR (booknews.com).
Author | : Anjaneyulu Marayya |
Publisher | : |
Total Pages | : 0 |
Release | : 2018-06 |
Genre | : Business & Economics |
ISBN | : 9788188449149 |
Download Quality Assurance And Quality Management In Pharmaceutical Industry Book in PDF, ePub and Kindle
QA is the most vital function of Total Quality Management (TQM) in pharmaceutical industry. This book presents the basic concepts on various topics like QMS, GLP, GMP, Quality Audit, Statistical Quality Control and analytica methods for QA. The elements, requirement and interpretation of ISO 9000 series of QMS are presented in detail.
Author | : Dr. Santosh Karajgi , Dr. Shripad S Potadar , Dr. Sudha Patil , Mr. Ajay Shahapur , Ms. Maharani H Bhandarakavathe |
Publisher | : Shashwat Publication |
Total Pages | : 290 |
Release | : 2024-05-07 |
Genre | : Medical |
ISBN | : 936087258X |
Download Pharmaceutical Quality Assurance: A Textbook Book in PDF, ePub and Kindle
The Pharmacy Council of India's (PCI) revised B. Pharmacy syllabus is followed in this state-of-the-art book. The broader topics of pharmaceutical quality assurance that undergrads, postgrads, industry professionals, researchers, and students getting ready for different competitive tests need to be covered in this book's encompassing content. The writing style of this book is clear, straightforward, and uncomplicated, which sets it apart from others. For the self-evolution of learning, the book is complemented by questions in the formats of multiple choice, fill in the blank, true-false, short answer, and long answer. Additionally included are the solutions to the True-False, Fill in the Blank, and Multiple-Choice problems. Links to websites and recommended reading are provided to assist readers in staying up to date on the most recent advancements in the field of pharmaceutical quality assurance. The book can be used as the main source of instruction or as supplementary material by academicians and teachers at universities and colleges for undergraduate and graduate pharmacy courses.
Author | : David Roesti |
Publisher | : John Wiley & Sons |
Total Pages | : 594 |
Release | : 2020-01-02 |
Genre | : Technology & Engineering |
ISBN | : 1119356075 |
Download Pharmaceutical Microbiological Quality Assurance and Control Book in PDF, ePub and Kindle
Relying on practical examples from the authors’ experience, this book provides a thorough and modern approach to controlling and monitoring microbial contaminations during the manufacturing of non-sterile pharmaceuticals. Offers a comprehensive guidance for non-sterile pharmaceuticals microbiological QA/QC Presents the latest developments in both regulatory expectations and technical advancements Provides guidance on statistical tools for risk assessment and trending of microbiological data Describes strategy and practical examples from the authors’ experience in globalized pharmaceutical companies and expert networks Offers a comprehensive guidance for non-sterile pharmaceuticals microbiological QA/QC Presents the latest developments in both regulatory expectations and technical advancements Provides guidance on statistical tools for risk assessment and trending of microbiological data Describes strategy and practical examples from the authors’ experience in globalized pharmaceutical companies and expert networks
Author | : K P R Chowdary |
Publisher | : |
Total Pages | : 212 |
Release | : 2019-12-05 |
Genre | : Medical |
ISBN | : 9789389354966 |
Download A Textbook of Pharmaceutical Quality Assurance Book in PDF, ePub and Kindle
Author | : G Welty |
Publisher | : Elsevier |
Total Pages | : 374 |
Release | : 2013-06-30 |
Genre | : Medical |
ISBN | : 190881862X |
Download Quality Assurance Book in PDF, ePub and Kindle
Quality assurance is necessary to maintain quality and services in the pharmaceutical and life science industries. Quality assurance demonstrates that the logic and practice of problem solving can integrate both program efficacy and regulatory compliance. This title is divided into three parts; the first part discusses the process by which a problem in regulated industry is identified, for example a manufacturing deviation that leads to an adulterated drug product, and reviews the decision-making steps involved in remedying the problem. The second part delves into the staff training requirements of procedures that are thereby revised. The third part expands on this discussion by considering piloting the proposed training module, preparing assessments of trainee proficiency, evaluating the training module, including integrating rigorous evaluative designs with formative program improvement, and documenting the entire effort. Presents a comprehensive view of the field of quality assurance An approach grounded in direct experience Uses diagrams and figures to clarify analytical points
Author | : Steve L. Nail |
Publisher | : Springer Science & Business Media |
Total Pages | : 479 |
Release | : 2012-12-06 |
Genre | : Medical |
ISBN | : 1461505496 |
Download Development and Manufacture of Protein Pharmaceuticals Book in PDF, ePub and Kindle
In this era of biotechnology there have been many books covering the fundamentals of recombinant DNA technology and protein chemistry. However, not many sources are available for the pharmaceutical develop ment scientist and other personnel responsible for the commercialization of the finished dosage forms of these new biopharmaceuticals and other products from biotechnology. This text will help to fill this gap. Once active biopharmaceutical molecules are candidates for clinical trial investigation and subsequent commercialization, a number of other activities must take place while research and development on these molecules continues. The active ingredient itself must be formulated into a finished dosage form that can be conveniently used by health care professionals and patients. Properties of the biopharmaceutical molecule must be clearly understood so that the appropriate finished product formulation can be developed. Finished product formulation development includes not only the chemical formulation, but also the packaging system, the manufacturing process, and appropriate control strategies to assure such good manufacturing practice attributes as safety, identity, strength, purity, and quality.