Nonclinical Statistics for Pharmaceutical and Biotechnology Industries
Title | Nonclinical Statistics for Pharmaceutical and Biotechnology Industries PDF eBook |
Author | Lanju Zhang |
Publisher | Springer |
Total Pages | 698 |
Release | 2016-01-13 |
Genre | Medical |
ISBN | 3319235583 |
This book serves as a reference text for regulatory, industry and academic statisticians and also a handy manual for entry level Statisticians. Additionally it aims to stimulate academic interest in the field of Nonclinical Statistics and promote this as an important discipline in its own right. This text brings together for the first time in a single volume a comprehensive survey of methods important to the nonclinical science areas within the pharmaceutical and biotechnology industries. Specifically the Discovery and Translational sciences, the Safety/Toxiology sciences, and the Chemistry, Manufacturing and Controls sciences. Drug discovery and development is a long and costly process. Most decisions in the drug development process are made with incomplete information. The data is rife with uncertainties and hence risky by nature. This is therefore the purview of Statistics. As such, this book aims to introduce readers to important statistical thinking and its application in these nonclinical areas. The chapters provide as appropriate, a scientific background to the topic, relevant regulatory guidance, current statistical practice, and further research directions.
Statistics for Biotechnology Process Development
Title | Statistics for Biotechnology Process Development PDF eBook |
Author | Todd Coffey |
Publisher | CRC Press |
Total Pages | 402 |
Release | 2018-05-16 |
Genre | Mathematics |
ISBN | 1351646346 |
Written specifically for biotechnology scientists, engineers, and quality professionals, this book describes and demonstrates the proper application of statistical methods throughout Chemistry, Manufacturing, and Controls (CMC). Filled with case studies, examples, and easy-to-follow explanations of how to perform statistics in modern software, it is the first book on CMC statistics written primarily for practitioners. While statisticians will also benefit from this book, it is written particularly for industry professionals who don’t have access to a CMC statistician or who want to be more independent in the design and analysis of their experiments. Provides an introduction to the statistical concepts important in the biotechnology industry Focuses on concepts with theoretical details kept to a minimum Includes lots of real examples and case studies to illustrate the methods Uses JMP software for implementation of the methods Offers a text suitable for scientists in the industry with some quantitative training Written and edited by seasoned veterans of the biotechnology industry, this book will prove useful to a wide variety of biotechnology professionals. The book brings together individual chapters that showcase the use of statistics in the most salient areas of CMC.
The Application of Statistical Process Control in the Pharmaceutical and Biotechnology Industries
Title | The Application of Statistical Process Control in the Pharmaceutical and Biotechnology Industries PDF eBook |
Author | T Cochrane |
Publisher | Elsevier |
Total Pages | 0 |
Release | 2029-01-01 |
Genre | Medical |
ISBN | 9781908818362 |
Innovative new technology now allows the measurement and collection of data throughout many manufacturing processes previously unavailable. The The Application of Statistical Process Control in the Pharmaceutical and Biotechnology Industries is a starting point for anyone who has been tasked to use technology to measure and collect data to gain an understanding of their processes in order to improve and control lengthy, complex supply chains in the pharmaceutical industry. It is a practical guide on how to apply statistical process control (SPC) within the pharmaceutical industry. It encourages all those involved in the industry - whether it be production, quality or the regulatory bodies - to start assessing data in a different way. This book delivers a way of viewing data that is both simple and easy to understand and relates to our understanding of the world in which we work. The first book to describe SPC in the pharmaceutical and biotechnology industries Highly practical approach Contains many case studies showing the application of SPC
Emerging Non-Clinical Biostatistics in Biopharmaceutical Development and Manufacturing
Title | Emerging Non-Clinical Biostatistics in Biopharmaceutical Development and Manufacturing PDF eBook |
Author | Harry Yang |
Publisher | CRC Press |
Total Pages | 278 |
Release | 2016-11-30 |
Genre | Mathematics |
ISBN | 1315354454 |
The premise of Quality by Design (QbD) is that the quality of the pharmaceutical product should be based upon a thorough understanding of both the product and the manufacturing process. This state-of-the-art book provides a single source of information on emerging statistical approaches to QbD and risk-based pharmaceutical development. A comprehensive resource, it combines in-depth explanations of advanced statistical methods with real-life case studies that illustrate practical applications of these methods in QbD implementation.
Pharmaceutical Statistics
Title | Pharmaceutical Statistics PDF eBook |
Author | T E Gopala Krishna Murty |
Publisher | Pharmamed Press |
Total Pages | 492 |
Release | 2016-10 |
Genre | Medical |
ISBN | 9789385433795 |
Books covering pharmaceutical sciences combined with statistics are not available in the market. To overcome this setback, this book is authored in a detailed and easy to understand manner incorporating the updated information containing the following features. Syllabus prescribed for B. Pharm & M. Pharm students is covered in detail The application of pharmaceutical statistics to research and clinical evaluation Prime importance is given to the creation of tables and graphs Data presentation, inferential tests such as parametric and nonparametric methods, regression and correlation factors are presented lucidly The importance of ANOVA in statistical designs used in pharmaceutical research Introduction of elementary concepts of the design and analysis of factorial designs Optimization techniques with suitable examples The important designs and their applications predominantly used in controlled clinical studies Application of statistics in quality control.
Essential Statistics for the Pharmaceutical Sciences
Title | Essential Statistics for the Pharmaceutical Sciences PDF eBook |
Author | Philip Rowe |
Publisher | John Wiley & Sons |
Total Pages | 432 |
Release | 2015-07-20 |
Genre | Medical |
ISBN | 1118913418 |
Essential Statistics for the Pharmaceutical Sciences is targeted at all those involved in research in pharmacology, pharmacy or other areas of pharmaceutical science; everybody from undergraduate project students to experienced researchers should find the material they need. This book will guide all those who are not specialist statisticians in using sound statistical principles throughout the whole journey of a research project - designing the work, selecting appropriate statistical methodology and correctly interpreting the results. It deliberately avoids detailed calculation methodology. Its key features are friendliness and clarity. All methods are illustrated with realistic examples from within pharmaceutical science. This edition now includes expanded coverage of some of the topics included in the first edition and adds some new topics relevant to pharmaceutical research. a clear, accessible introduction to the key statistical techniques used within the pharmaceutical sciences all examples set in relevant pharmaceutical contexts. key points emphasised in summary boxes and warnings of potential abuses in ‘pirate boxes’. supplementary material - full data sets and detailed instructions for carrying out analyses using packages such as SPSS or Minitab – provided at: https://www.wiley.com/go/rowe/statspharmascience2e An invaluable introduction to statistics for any science student and an essential text for all those involved in pharmaceutical research at whatever level.
Handbook of Pharmaceutical Biotechnology
Title | Handbook of Pharmaceutical Biotechnology PDF eBook |
Author | Jay P Rho |
Publisher | CRC Press |
Total Pages | 214 |
Release | 2003-03-31 |
Genre | Medical |
ISBN | 9780789016355 |
Stay up to date with changes in the biopharmaceutical products market! With the growth rate of biopharmaceutical products ascending rapidly since the 1980s, the number of biotechnology companies has risen to more than 1200 new businesses in the Unites States alone. This dramatic increase creates a new set of challenges in education, putting demands on teachers and students to keep pace with innovations in terminology and techniques. The Handbook of Pharmaceutical Biotechnology is essential in meeting those challenges. A practical compendium of biotechnology-produced drugs, the Handbook of Pharmaceutical Biotechnology covers general principles of biotechnology and pharmaceuticals, putting usable information in the hands of those who need it most. The book presents descriptions that break down each pharmaceutical product by pharmacology, pharmacokinetics, clinical applications, toxicities, and dosage guidelines. It also reviews prescription products, discussing clinical uses and trials, adverse reactions, and more. Tables, figures, and extensive references add to each comprehensive summary. The Handbook of Pharmaceutical Biotechnology also includes up-to-date information on: monoclonal antibodies (Abciximab, Muromonab-CD3) enzymes and regulators of enzyme activity (Alteplase, clotting factors, Dornase alpha) anticytokines olgonucleotide and gene therapy hematopoietic growth factors (interleukins, interferons, colony stimulating factors, erythropoietin) As the worldwide production and sales of biotechnology-derived pharmaceuticals and diagnostics continues to grow, teachers, students, and clinical pharmacists need to maintain a clear and current understanding of the field. The Handbook of Pharmaceutical Biotechnology presents a thoughtful and thorough guide to keeping pace in this evolving industry.