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...


“eric c ford, phd”

Showing 1 - 12 of 12 results for “eric c ford, phd”
Skip side bar filters

  • Quality and Safety in Radiation Oncology

    Implementing Tools and Best Practices for Patients, Providers, and Payers

    Edited by Adam P. Dicker, MD, PhD, Eric C. Ford, PhD, Tim R. Williams, MD ...
    Quality and Safety in Radiation Oncology is the first book to provide an authoritative and evidence-based guide to the understanding and implementation of quality and safety procedures in radiation oncology practice. Alongside the rapid growth of technology and radiotherapy treatment options for cancer in recent years, quality and safety standards are not only of the utmost importance but best ... Read more

    $109.59 CAD

People who read this also enjoyed

  • Clinical Research Coordinator Handbook, Fourth Edition

    by Deborah Norris ...
    In this fully revised and expanded fourth edition of the essential reference for clinical research coordinators, Deborrah Norris provides expanded coverage of CRC duties and regulatory requirements, including new sections on investigator responsibilities, data clarification, and adverse event reporting. The books five appendices include a directory of CRC resources, updated forms and checklists, ... Read more

    $9.61 CAD or Free with Kobo Plus

  • 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

    $110.39 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

  • Clinical Engineering Handbook

    Edited by Joseph Dyro ...
    As the biomedical engineering field expands throughout the world, clinical engineers play an evermore-important role as translators between the medical, engineering, and business professions. They influence procedure and policy at research facilities, universities, as well as private and government agencies including the Food and Drug Administration and the World Health Organization. The ... Read more

    $167.99 CAD

  • Translational Neuroscience

    A Guide to a Successful Program

    Edited by Edgar Garcia-Rill ...
    Translational research looks to take the latest innovations made in the laboratory setting to translate findings into effective and sustainable medical interventions and improved preventative measures. Funding support is increasingly tied to practical healthcare outcomes, with this trend likely only to increase in coming years, Translational Neuroscience: A Guide to a Successful Program, is a ... Read more

    $113.99 CAD

  • Pharmaceutical Quality by Design

    A Practical Approach

    Edited by Walkiria S. Schlindwein, Mark Gibson ...
    Series series Advances in Pharmaceutical Technology
    A practical guide to Quality by Design for pharmaceutical product developmentPharmaceutical Quality by Design: A Practical Approach outlines a new and proven approach to pharmaceutical product development which is now being rolled out across the pharmaceutical industry internationally. Written by experts in the field, the text explores the QbD approach to product development. This innovative ... Read more

    $108.99 CAD

  • Risk Management Applications in Pharmaceutical and Biopharmaceutical Manufacturing

    Edited by Hamid Mollah, Harold Baseman, Mike Long ...
    Series Book 4 - Wiley Series in Biotechnology and Bioengineering
    Sets forth tested and proven risk management practices in drug manufacturingRisk management is essential for safe and efficient pharmaceutical and biopharmaceutical manufacturing, control, and distribution. With this book as their guide, readers involved in all facets of drug manufacturing have a single, expertly written, and organized resource to guide them through all facets of risk management ... Read more

    $163.99 CAD

  • Risk, Error and Uncertainty: Laboratory Quality Management in the Age of Metrology, An Issue of the Clinics in Laboratory Medicine

    by David Armbruster, James O. Westgard, Ph.D., FACB, Sten Westgard, MS ...
    Series Book Volume 37-1 - The Clinics: Internal Medicine
    This issue of Clinics in Laboratory Medicine entitled “Risk, Error and Uncertainty: Laboratory Quality Management in the Age of Metrology will be guest edited by Sten Westgard, James Westgard, and David Armbruster. The issue will cover a broad range of topics related to management in the laboratory including but not limited to: Metrology Perspectives; Biologic Variation Approach to Daily ... Read more

    $92.39 CAD

  • 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

    $131.99 CAD

  • Principles and Practice of Clinical Research

    Edited by John I. Gallin, Frederick P Ognibene, Laura Lee Johnson ...
    Principles and Practice of Clinical Research, Fourth Edition has been thoroughly revised to provide a comprehensive look at both the fundamental principles and expanding practice of clinical research. New to this edition of this highly regarded reference, authors have focused on examples that broadly reflect clinical research on a global scale while including a discussion of international ... Read more

    $110.39 CAD

  • Specification of Drug Substances and Products

    Development and Validation of Analytical Methods

    Edited by Thomas W. Rosanske, Christopher M. Riley ...
    Specification of Drug Substances and Products: Development and Validation of Analytical Methods is a comprehensive and critical analysis of the requirements and approaches to setting specifications for new pharmaceutical products, with an emphasis on phase-appropriate development and validation of analytical methods. This book is intended as more than a review of new regional guidelines, existing ... Read more

    $106.39 CAD