Skip to main content
Search Button
Canada Kobo store Gift Cards Help

Rakuten Kobo

Wishlist

Shopping Cart

You're getting the VIP treatment!

Item(s) unavailable for purchase
Please review your cart. You can remove the unavailable item(s) now or we'll automatically remove it at Checkout.
itemsitem
itemsitem

Recommended For You

Loading...


Top Series in Canada

Showing 1 - 12 of 12 results for “bharat jasani”
Skip side bar filters

  • Precision Cancer Medicine

    Role of the Pathologist

    by Bharat Jasani, Ralf Huss, Clive R. Taylor ...
    Series series Medicine (R0)
    This book describes the changing role of pathology in aiding reproducible and accurate patient selection for predictive cancer therapy. Particular attention is given to the clinical application of cutting-edge cancer biomarkers to accurately select patients for targeted cancer therapy and how artificial intelligence can improve the precision of treatments. The advent and basis of predictive cancer ... Read more

    $128.99 CAD

People who read this also enjoyed

  • A Comprehensive Guide to Toxicology in Preclinical Drug Development

    Edited by Ali S. Faqi ...
    A Comprehensive Guide to Toxicology in Preclinical Drug Development is a resource for toxicologists in industry and regulatory settings, as well as directors working in contract resource organizations, who need a thorough understanding of the drug development process. Incorporating real-life case studies and examples, the book is a practical guide that outlines day-to-day activities and ... Read more

    $176.79 CAD

  • Early Drug Development

    Strategies and Routes to First-in-Human Trials

    Edited by Mitchell N. Cayen ...
    The focus of early drug development has been the submission of an Investigational New Drug application to regulatory agencies. Early Drug Development: Strategies and Routes to First-in-Human Trials guides drug development organizations in preparing and submitting an Investigational New Drug (IND) application. By explaining the nuts and bolts of preclinical development activities and their ... Read more

    $215.99 CAD

  • Principles of Clinical Pharmacology

    Edited by Shiew-Mei Huang, Juan J.L. Lertora, Arthur J. Atkinson Jr. ...
    Principles of Clinical Pharmacology is a successful survey covering the pharmacologic principles underlying the individualization of patient therapy and contemporary drug development. This essential reference continues to focus on the basics of clinical pharmacology for the development, evaluation, and clinical use of pharmaceutical products while also addressing the most recent advances in the ... Read more

    $110.39 CAD

  • Pharmaceutical Toxicology in Practice

    A Guide to Non-clinical Development

    Edited by Alberto Lodola, Jeanne Stadler ...
    This book describes, with references to key source materials, the background to, and conduct of, the principal nonclinical studies that are central to drug development. The chapters provide an understanding of the key components of the preclinical phase of drug development with a hands-on description, with core chapters addressing study conduct, types, and reporting. As such, it is a practical ... Read more

    $145.99 CAD

  • Radiomics and Its Clinical Application

    Artificial Intelligence and Medical Big Data

    by Jie Tian, Di Dong, Zhenyu Liu, Jingwei Wei ...
    Series series The MICCAI Society book Series
    The rapid development of artificial intelligence technology in medical data analysis has led to the concept of radiomics. This book introduces the essential and latest technologies in radiomics, such as imaging segmentation, quantitative imaging feature extraction, and machine learning methods for model construction and performance evaluation, providing invaluable guidance for the researcher ... Read more

    $110.39 CAD

  • Clinical Trials

    Study Design, Endpoints and Biomarkers, Drug Safety, and FDA and ICH Guidelines

    by Tom Brody ...
    Clinical Trials: Study Design, Endpoints and Biomarkers, Drug Safety, and FDA and ICH Guidelines is a practical guidebook for those engaged in clinical trial design. This book details the organizations and content of clinical trials, including trial design, safety, endpoints, subgroups, HRQoL, consent forms and package inserts. It provides extensive information on both US and international ... Read more

    $71.19 CAD

  • Flow Cytometry in Drug Discovery and Development

    Edited by Virginia Litwin, Philip Marder ...
    This book covers the unique application of flow cytometry in drug discovery and development. The first section includes two introductory chapters, one on flow cytometry and one on biomarkers, as well as a chapter on recent advances in flow cytometry. The second section focuses on the unique challenges and added benefits associated with the use of flow cytometry in the drug development process. The ... Read more

    $167.99 CAD

  • Imaging Biomarkers

    Development and Clinical Integration

    Edited by Luis Martí-Bonmatí, Angel Alberich-Bayarri ...
    Series series Medicine (R0)
    This is the first book to cover all aspects of the development of imaging biomarkers and their integration into clinical practice, from the conceptual basis through to the technical aspects that need to be considered in order to ensure that medical imaging can serve as a powerful quantification instrument capable of providing valuable information on organ and tissue properties. The process of ... Read more

    $109.99 CAD

  • Clinical Trials

    Study Design, Endpoints and Biomarkers, Drug Safety, and FDA and ICH Guidelines

    by Tom Brody ...
    Clinical Trials, Second Edition, offers those engaged in clinical trial design a valuable and practical guide. This book takes an integrated approach to incorporate biomedical science, laboratory data of human study, endpoint specification, legal and regulatory aspects and much more with the fundamentals of clinical trial design. It provides an overview of the design options along with the ... Read more

    $88.79 CAD

  • Drug Discovery Toxicology

    From Target Assessment to Translational Biomarkers

    Edited by J. Eric McDuffie, Andrew J. Olaharski, Brandon D. Jeffy, Yvonne Will ...
    As a guide for pharmaceutical professionals to the issues and practices of drug discovery toxicology, this book integrates and reviews the strategy and application of tools and methods at each step of the drug discovery process.• Guides researchers as to what drug safety experiments are both practical and useful• Covers a variety of key topics – safety lead optimization, in vitro-in vivo ... Read more

    $234.99 CAD

  • Physiologically Based Pharmacokinetic (PBPK) Modeling and Simulations

    Principles, Methods, and Applications in the Pharmaceutical Industry

    by Sheila Annie Peters ...
    Physiologically Based Pharmacokinetic (PBPK) Modeling and SimulationsThe first book dedicated to the emerging field of physiologically based pharmacokinetic modeling (PBPK)Now in its second edition, Physiologically Based Pharmacokinetic (PBPK) Modelling and Simulations: Principles, Methods, and Applications in the Pharma Industry remains the premier reference book throughout the rapidly growing ... Read more

    $207.99 CAD