Skip to main content
Search Button
United States 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...


“jonathan van niewaal”

Showing 1 - 12 of 12 results for “jonathan van niewaal”
Skip side bar filters

  • Biomarkers in Drug Discovery and Development

    A Handbook of Practice, Application, and Strategy

    Edited by Ramin Rahbari, Jonathan Van Niewaal, Michael R. Bleavins ...
    This book continues the legacy of a well-established reference within the pharmaceutical industry – providing perspective, covering recent developments in technologies that have enabled the expanded use of biomarkers, and discussing biomarker characterization and validation and applications throughout drug discovery and development.Explains where proper use of biomarkers can substantively impact ... Read more

    $191.00 USD

People who read this also enjoyed

  • Principles of Clinical Pharmacology

    Edited by Darrell R. Abernethy, Charles E. Daniels, Robert Dedrick, Sanford P. Markey, Arthur J. Atkinson Jr. ...
    This revised second edition covers the pharmacologic principles underlying the individualization of patient therapy and contemporary drug development, focusing on the fundamentals that underlie the clinical use and contemporary development of pharmaceuticals. Authors drawn from academia, the pharmaceutical industry and government agencies cover the spectrum of material, including pharmacokinetic ... Read more

    $115.19 USD

  • Principles and Practice of Clinical Research

    Edited by Frederick P Ognibene, John I. Gallin ...
    The third edition of this innovative work again provides a unique perspective on the clinical discovery process by providing input from experts within the NIH on the principles and practice of clinical research. Molecular medicine, genomics, and proteomics have opened vast opportunities for translation of basic science observations to the bedside through clinical research. As an introductory ... Read more

    $112.49 USD

  • 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

    $179.99 USD

  • 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

    $161.00 USD

  • 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

    $112.49 USD

  • 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

    $113.00 USD

  • 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

    $71.99 USD

  • Clinical and Translational Science

    Principles of Human Research

    Edited by David Robertson, Gordon H. Williams ...
    Clinical or translational science is the field of study devoted to investigating human health and disease, interventions and outcomes for the purposes of developing new treatment approaches, devices, and modalities to improve health. New molecular tools and diagnostic technologies based on clinical and translational research have lead to a better understanding of human disease and the application ... Read more

    $123.29 USD

  • 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

    $89.99 USD

  • 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

    $129.00 USD

  • 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

    $181.00 USD