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000753424 019__ $$a935272706$$a935640040
000753424 020__ $$a9783319235585$$q(electronic book)
000753424 020__ $$a3319235583$$q(electronic book)
000753424 020__ $$z9783319235578
000753424 0247_ $$a10.1007/978-3-319-23558-5$$2doi
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000753424 24500 $$aNonclinical statistics for pharmaceutical and biotechnology industries$$h[electronic resource] /$$cLanju Zhang, editor ; Max Kuhn, Ian Peers, Stan Altan, section editors.
000753424 264_1 $$aCham :$$bSpringer,$$c2016.
000753424 300__ $$a1 online resource (xxii, 698 pages) :$$billustrations.
000753424 336__ $$atext$$btxt$$2rdacontent
000753424 337__ $$acomputer$$bc$$2rdamedia
000753424 338__ $$aonline resource$$bcr$$2rdacarrier
000753424 4901_ $$aStatistics for biology and health,$$x1431-8776
000753424 500__ $$aIncludes index.
000753424 5050_ $$aIntroduction to Nonclinical Statistics for Pharmaceutical and Biotechnology Industries -- Regulatory Nonclinical Statistics -- How to be a good nonclinical statistician -- Statistical Methods for Drug Discovery -- High-throughput Screening Data Analysis -- Quantitative-Structure Activity Relationship Modeling and Cheminformatics -- GWAS for Drug Discovery -- Statistical applications in Design and Analysis of In-Vitro Safety Screening Assays -- Nonclinical safety assessment: an introduction for statisticians -- General Toxicology, Safety Pharmacology, Reproductive Toxicology and Juvenile Toxicology Studies -- Clinical Assays for Biological Macromolecules -- Recent Research Projects by FDA's Pharmacology and Toxicology Statistics Team -- Design and evaluation of drug combination studies -- Biomarkers -- Overview of Drug Development and Statistical Tools for Manufacturing and Testing -- Assay Validation -- Lifecycle Approach to Bioassay -- Quality by Design: Building Quality into Products and Processes -- Process Validation -- Acceptance Sampling -- Process Capability and Statistical Process Control -- Statistical Considerations for Stability and the Estimation of Shelf Life.- In Vitro Dissolution Testing: Statistical Approaches and Issues -- Assessing Content Uniformity -- Chemometrics and Predictive Modelling -- Statistical Methods for Comparability Studies.
000753424 506__ $$aAccess limited to authorized users.
000753424 520__ $$aThis 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.
000753424 588__ $$aOnline resource; title from PDF title page (SpringerLink, viewed January 21, 2016).
000753424 650_0 $$aPharmacology$$xStatistical methods.
000753424 650_0 $$aBiotechnology$$xStatistical methods.
000753424 7001_ $$aZhang, Lanju,$$eeditor.
000753424 77608 $$iPrint version:$$z9783319235578
000753424 830_0 $$aStatistics for biology and health.
000753424 852__ $$bebk
000753424 85640 $$3SpringerLink$$uhttps://univsouthin.idm.oclc.org/login?url=http://link.springer.com/10.1007/978-3-319-23558-5$$zOnline Access$$91397441.1
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