Current Topics in Nonclinical Drug Development Series – serie
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3 produkter
3 produkter
2 693 kr
Skickas inom 10-15 vardagar
The inaugural volume in the Current Topics in Nonclinical Drug Development Series explores the critical issues and current topics in nonclinical drug development. This first volume covers individual topics and strategies in drug development from compound characterization to drug registration. Written by a variety of experts in the field, recent and rapid advances in technologies and associated changes in regulatory guidance are discussed.Additional features include: Deals with day-to-day issues in study design, evaluation of findings, and presentation of data. Explains new approaches in the development of medical devices. Includes dedicated chapters on the use of bioinformatics in drug development. Addresses strategies for photosafety testing of drugs.Current Topics in Nonclinical Drug Development, Volume I will aid toxicologists, toxicologic pathologists, consultants, regulators, Study Directors, and nonclinical scientists dealing with day-to-day issues in study design, evaluation of findings, and presentation of data. In addition, the book will be a valuable reference for academicians and graduate students pursuing research related to nonclinical drug development.
2 622 kr
Skickas inom 10-15 vardagar
The second volume in the CURRENT TOPICS IN NONCLINICAL DRUG DEVELOPMENT SERIES explores the critical issues and current topics in nonclinical drug development. This second volume covers individual topics and strategies in drug development from compound characterization to drug registration. Written by a variety of experts in the field, recent and rapid advances in technologies and associated changes in regulatory guidance are discussed.Select topics include:Evolution of Artificial Intelligence (AI) technologies and the impact on toxicologic pathology.Current approaches to carcinogenicity testing.Predicting drug-drug interactions.Current understanding of idiosyncratic drug reaction.Assessing cardiovascular risks beyond QT interval.Use of 3D cell cultures in toxicology and ADME.Development of small molecule-antibody complexes.Differentiating adverse from non-adverse findings in nonclinical studies.Current Topics in Nonclinical Drug Development: Volume 2 will aid toxicologists, toxicologic pathologists, consultants, regulators, study directors, and nonclinical scientists dealing with day-to-day issues encountered in drug development and assist in formulating strategies for resolution of these issues. In addition, the book will be a valuable reference for academicians and graduate students pursuing research related to nonclinical drug development.
3 150 kr
Kommande
This third volume in the series focuses on such germane issues as the weight of evidence approach, the 3Rs, (Replacement, Reduction, and Refinement) personalized drug therapies, and oncology therapeutics, among others. Volumes in this series are aimed at toxicologists and toxicologic pathologists involved in drug development. Volumes in the Current Topics in Nonclinical Drug Development series are aimed at toxicologists, toxicologic pathologists, regulators, and study directors, dealing with issues in study design, evaluation of findings, and presentation of data. In addition, the series will serve as an aid to academicians and graduate students studying nonclinical drug development.Key Features:Explores the critical issues and current topics important in nonclinical drug developmentDeals with day-to-day issues in study design, evaluation of findings, and presentation of dataAids academicians and graduate students pursuing research related to nonclinical drug developmentDelves into both the art and science of nonclinical drug development and its impact on translational medicine and human safety