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Top Series in United States

Showing 1 - 12 of 12 results for “duncan low”
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  • Improving the Psychological Wellbeing of Children and Young People

    Effective Prevention and Early Intervention Across Health, Education and Social Care

    by Duncan Law, Iyabo Fatimilehin, Laura Casale, Sally Zlotowitz, Natalie Seymour, Mark Moubarak Chentite, Ruth Butterworth, Ruth O'Shaughnessy, Michael Galbraith, Caroline White, Waveney Patel, Anna Picciotto, Joe Hickey, Jaime Craig, Sara O'Curry, Sally Benson, Jenny Taylor, Lisa Shostak ...
    Written for professionals spanning children's services, this must-read guide provides an authoritative overview of what shapes the psychological wellbeing of children and young people - from perinatal care and adverse childhood experiences (ACEs) through to their socioeconomic circumstances, schools and the wider community.Contributors provide a concise overview of the evidence base, identifying ... Read more

    $28.69 USD

  • Working with Goals in Psychotherapy and Counselling

    Edited by Duncan Law, Mick Cooper ...
    Recent evidence has shown that the successful setting of goals brings about positive outcomes in psychological therapy. Goals help to focus and direct clients' and therapists' attention in therapeutic work. They also engender hope and help energise clients. No longer are clients victims of their circumstances, but through goal setting they become people who have the potential to act towards and ... Read more

    $46.79 USD

  • PAT Applied in Biopharmaceutical Process Development And Manufacturing

    An Enabling Tool for Quality-by-Design

    Edited by Cenk Undey, Duncan Low, Jose C. Menezes, Mel Koch ...
    Series series Biotechnology and Bioprocessing
    As with all of pharmaceutical production, the regulatory environment for the production of therapeutics has been changing as a direct result of the US FDA-initiated Quality by Design (QbD) guidelines and corresponding activities of the International Committee for Harmonization (ICH). Given the rapid growth in the biopharmaceutical area and the comp ... Read more

    $325.00 USD

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  • Bioreactors

    Design, Operation and Novel Applications

    by Carl-Fredrik Mandenius ...
    In this expert handbook both the topics and contributors are selected so as to provide an authoritative view of possible applications for this new technology. The result is an up-to-date survey of current challenges and opportunities in the design and operation of bioreactors for high-value products in the biomedical and chemical industries.Combining theory and practice, the authors explain such ... Read more

    $149.00 USD

  • 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

    $90.00 USD

  • Biomechatronic Design in Biotechnology

    A Methodology for Development of Biotechnological Products

    by Carl-Fredrik Mandenius, Mats Björkman ...
    “… a must-read for all modern bio-scientists and engineers working in the field of biotechnology.” – Biotechnology Journal, 2012, 7A cutting-edge guide on the fundamentals, theory, and applications of biomechatronic design principlesBiomechatronic Design in Biotechnology presents a complete methodology of biomechatronics, an emerging variant of the mechatronics field that marries biology, ... Read more

    $95.00 USD

  • 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

    $107.99 USD

  • Extractables and Leachables

    Characterization of Drug Products, Packaging, Manufacturing and Delivery Systems, and Medical Devices

    by Dennis Jenke ...
    EXTRACTABLES AND LEACHABLESLearn to address the safety aspects of packaged drug products and medical devicesPharmaceutical drug products and medical devices are expected to be effective and safe to use. This includes minimizing patient, user or product exposure to impurities leached from these items when the drug product is administered or when the medical device is used. Clearly, patient or user ... Read more

    $161.00 USD

  • ICH Quality Guidelines

    An Implementation Guide

    Edited by David Elder, Raymond W. Nims, Andrew Teasdale ...
    Examining the implications and practical implementation of multi-disciplinary International Conference on Harmonization (ICH) topics, this book gives an integrated view of how the guidelines inform drug development strategic planning and decision-making.• Addresses a consistent need for interpretation, training, and implementation examples of ICH guidelines via case studies• Offers a primary ... Read more

    $309.00 USD

  • Modern Pharmaceutics

    by D. K. Tripathi ...
    "Modern Pharmaceutics" is a must-read book for students pursuing M. Pharmacy in Pharmaceutics. The book covers the curriculum and syllabus developed by the Pharmacy Council of India, providing students with the necessary knowledge and skills required in the field of pharmaceutical services.The author has meticulously explained each topic and sub-topic systematically and logically. The book covers ... Read more

    $70.00 USD or Free with Kobo Plus

  • Comprehensive Two Dimensional Gas Chromatography

    Edited by Lourdes Ramos ...
    Series Book 55 - Comprehensive Analytical Chemistry
    The book reviews the basic concepts and highlights the most relevant advances and developments that have taken place in the field of comprehensive two dimensional gas chromatography (GC x GC) since its introduction in 1991. The several instrumental and technical approaches assayed and developed during these seventeen years and that have contributed to the development of this powerful separation ... Read more

    $287.99 USD

  • How to Develop Robust Solid Oral Dosage Forms

    From Conception to Post-Approval

    by Bhavishya Mittal ...
    Series series Expertise in Pharmaceutical Process Technology
    How to Develop Robust Solid Oral Dosage Forms from Conception to Post-Approval uses a practical and hands-on approach to cover the development process of solid oral dosage forms in one single source. The book details all of the necessary steps from formulation through the post-approval phase and contains industry case studies, real world advice, and troubleshooting tips. By merging the latest ... Read more

    $62.99 USD