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...


“walter moos”

Showing 1 - 12 of 12 results for “walter moos”
Skip side bar filters

  • Managing the Drug Discovery Process

    Insights and advice for students, educators, and practitioners

    by Susan Miller, Walter Moos, Barbara Munk, Stephen Munk, Charles Hart, David Spellmeyer ...
    Managing the Drug Discovery Process, Second Edition thoroughly examines the current state of pharmaceutical research and development by providing experienced perspectives on biomedical research, drug hunting and innovation, including the requisite educational paths that enable students to chart a career path in this field. The book also considers the interplay of stakeholders, consumers, and drug ... Read more

    $202.49 USD

  • Managing the Drug Discovery Process

    How to Make It More Efficient and Cost-Effective

    by Walter Moos, Susan Miller, Stephen Munk, Barbara Munk ...
    Managing the Drug Discovery Process: How to Make It More Efficient and Cost-Effective thoroughly examines the current state of pharmaceutical research and development by providing chemistry-based perspectives on biomedical research, drug hunting and innovation. The book also considers the interplay of stakeholders, consumers, and the drug firm with attendant factors, including those that are ... Read more

    $188.99 USD

People who read these also enjoyed

  • Real World Drug Discovery

    A Chemist's Guide to Biotech and Pharmaceutical Research

    by Robert M. Rydzewski ...
    Drug discovery increasingly requires a common understanding by researchers of the many and diverse factors that go into the making of new medicines. The scientist entering the field will immediately face important issues for which his education may not have prepared him: project teams, patent law, consultants, target product profiles, industry trends, Gantt charts, target validation, ... Read more

    $80.09 USD

  • Rigor Mortis

    How Sloppy Science Creates Worthless Cures, Crushes Hope, and Wastes Billions

    by Richard Harris ...
    An essential book to understanding whether the new miracle cure is good science or simply too good to be trueAmerican taxpayers spend $30 billion annually funding biomedical research, but over half of these studies can't be replicated due to poor experimental design, improper methods, and sloppy statistics. Bad science doesn't just hold back medical progress, it can sign the equivalent of a death ... Read more

    $16.99 USD

  • Improving Oncology Worldwide

    Education, Clinical Research and Global Cancer Care

    Edited by Uta Schmidt-Straßburger ...
    Series series Medicine (R0)
    This open access book describes strategies and experiences of highly skilled professionals in improving oncology care worldwide.The book is structured into three main sections with several chapters each, reflecting the authors' individual, real-life experiences. It explores ways to improve oncology education and scientific training, how to set up and run a clinical research facility ethically and ... Read more

    Free

  • The Age of Scientific Wellness

    Why the Future of Medicine Is Personalized, Predictive, Data-Rich, and in Your Hands

    by Leroy Hood, Nathan Price ...
    **“If you want to understand how the latest advances in genomics and AI can completely transform your health, and to translate this promise into practical tools that you can apply today, read this book!”—Mark Hyman, author of *Young Forever *****“A must-read for understanding the new era of data-driven medicine.” —David Agus, New York Times bestselling author of *The End of Illness ***We are on ... Read more

    $16.59 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

  • Pharmacology, Doping and Sports

    A Scientific Guide for Athletes, Coaches, Physicians, Scientists and Administrators

    Edited by Jean L. Fourcroy ...
    The work of dope testers is constantly being obstructed by the development of ever harder-to-trace new forms of banned substances. Organisations such as the World Anti-Doping Association and the United States Anti-Doping Agency are pioneering cutting-edge techniques designed to keep competition at the highest level fair and safe, and must ensure that their drug testing laboratories adhere to the ... Read more

    $70.99 USD

  • Principles and Practice of Pharmaceutical Medicine

    Edited by Lionel D. Edwards, Anthony W. Fox, Peter D. Stonier ...
    The new edition of Principles and Practice of Pharmaceutical Medicine is a comprehensive reference guide to all aspects of pharmaceutical medicine. New content includes chapters and coverage on regulatory updates, increasing international harmonization, transitional and probabilistic approaches to drug development, the growing sophistication and regulatory importance of pharmacovigilance, ... Read more

    $300.00 USD

  • Global New Drug Development

    An Introduction

    by Jan A. Rosier, Mark A. Martens, Josse R. Thomas ...
    Series series ULLA Series in Pharmaceutical Sciences
    The development of new drugs is very complex, costly and risky. Its success is highly dependent on an intense collaboration and interaction between many departments within the drug development organization, external investigators and service providers, in constant dialogue with regulatory authorities, payers, academic experts, clinicians and patient organizations. Within the different phases of ... Read more

    $110.00 USD

  • Clinical Trials

    What Patients and Healthy Volunteers Need to Know

    by Lorna Speid, Ph.D ...
    Every year, hundreds of thousands of healthy volunteers and patients worldwide undertake the journey through the maze that can be clinical trials. Research participants take part in clinical trials for a variety of reasons. The healthy volunteers may be seeking extra money to pay off college tuition, or they may know someone who is suffering and would potentially benefit from the results of the ... Read more

    $18.99 USD

  • Basic Principles of Drug Discovery and Development

    by Benjamin E. Blass ...
    Basic Principles of Drug Discovery and Development presents the multifaceted process of identifying a new drug in the modern era, providing comprehensive explanations of enabling technologies such as high throughput screening, structure based drug design, molecular modeling, pharmaceutical profiling, and translational medicine, all areas that have become critical steps in the successful ... Read more

    $67.49 USD