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Meilleures séries dans ce pays : Canada

1-12 sur 12 résultats pour « yaser dahman »
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  • Introduction to Pharmaceutical Technology Development

    Journey from Lab to Shelf of Commercial Pharmaceutical Drugs

    par Yaser Dahman ...
    Introduction to Pharmaceutical Technology Development: Journey from Lab to Shelf of Commercial Pharmaceutical Drugs is a complete reference and learning resource for those working in pharmaceutics or aspiring to join the industry. The book provides a comprehensive view into all aspects of drug discovery, approval, and production. Using examples of well-known drugs and their journeys from lab to ... En savoir plus

    $132.99 CAD

  • Biomaterials Science and Technology

    Fundamentals and Developments

    par Yaser Dahman ...
    Biomaterials Science and Technology: Fundamentals and Developments presents a broad scope of the field of biomaterials science and technology, focusing on theory, advances, and applications. It reviews the fabrication and properties of different classes of biomaterials such as bioinert, bioactive, and bioresorbable, in addition to biocompatibility. It further details traditional and recent ... En savoir plus

    $107.17 CAD

  • Nanotechnology and Functional Materials for Engineers

    par Yaser Dahman ...
    Collections series Micro and Nano Technologies
    Nanotechnology and Functional Materials for Engineers focuses on key essentials and examples across the spectrum of nanomaterials as applied by engineers, including nanosensors, smart nanomaterials, nanopolymers, and nanotubes. Chapters cover their synthesis and characteristics, production methods, and applications, with specific sections exploring nanoelectronics and electro-optic nanotechnology, ... En savoir plus

    $115.99 CAD

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  • An Introduction to Pharmaceutical Sciences

    Production, Chemistry, Techniques and Technology

    par Jiben Roy ...
    Collections series Woodhead Publishing Series in Biomedicine
    This textbook is written as a unified approach to various topics, ranging from drug discovery to manufacturing, techniques and technology, regulation and marketing. The key theme of the book is pharmaceuticals - what every student of pharmaceutical sciences should know: from the active pharmaceutical ingredients to the preparation of various dosage forms along with the relevant chemistry, this ... En savoir plus

    $87.99 CAD

  • The Challenge of CMC Regulatory Compliance for Biopharmaceuticals

    par John Geigert ...
    This book highlights the challenges facing quality assurance/quality control (QA/QC) in today's biopharmaceutical environment and presents the strategic importance and value generated by QA/QC for their involvement in control of manufacturing. It will put into perspective the need for a graded approach to QA/QC from early clinical trials through market approval. Since the first edition published ... En savoir plus

    $217.99 CAD

  • Extractables and Leachables

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

    par 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 ... En savoir plus

    $203.99 CAD

  • Oral Controlled Release Formulation Design and Drug Delivery

    Theory to Practice

    Modifié par Hong Wen, Kinam Park ...
    This book describes the theories, applications, and challenges for different oral controlled release formulations. This book differs from most in its focus on oral controlled release formulation design and process development. It also covers the related areas like preformulation, biopharmaceutics, in vitro-in vivo correlations (IVIVC), quality by design (QbD), and regulatory issues. ... En savoir plus

    $159.99 CAD

  • ICH Quality Guidelines

    An Implementation Guide

    Modifié par 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 ... En savoir plus

    $414.99 CAD

  • Biopharmaceutical Processing

    Development, Design, and Implementation of Manufacturing Processes

    Modifié par Gunter Jagschies, Eva Lindskog, Karol Lacki, Parrish M. Galliher ...
    Biopharmaceutical Processing: Development, Design, and Implementation of Manufacturing Processes covers bioprocessing from cell line development to bulk drug substances. The methods and strategies described are essential learning for every scientist, engineer or manager in the biopharmaceutical and vaccines industry. The integrity of the bioprocess ultimately determines the quality of the product ... En savoir plus

    $327.99 CAD

  • Process Scale Purification of Antibodies

    Modifié par Uwe Gottschalk ...
    Promoting a continued and much-needed renaissance in biopharmaceutical manufacturing, this book covers the different strategies and assembles top-tier technology experts to address the challenges of antibody purification.• Updates existing topics and adds new ones that include purification of antibodies produced in novel production systems, novel separation technologies, novel antibody formats and ... En savoir plus

    $267.99 CAD

  • Handbook of Modern Pharmaceutical Analysis

    Modifié par Satinder Ahuja, Stephen Scypinski ...
    Collections Livre 3 - Separation Science and Technology
    This book describes the role modern pharmaceutical analysis plays in the development of new drugs. Detailed information is provided as to how the quality of drug products is assured from the point of discovery until the patient uses the drug. Coverage includes state-of-the-art topics such as analytics for combinatorial chemistry and high-throughput screening, formulation development, stability ... En savoir plus

    $225.99 CAD

  • How to Develop Robust Solid Oral Dosage Forms

    From Conception to Post-Approval

    par Bhavishya Mittal ...
    Collections 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 ... En savoir plus

    $62.99 CAD