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  • Advancements in Fused Deposition Modeling (FDM)Technology for Pharmaceutical and Medical Applications

    In the rapidly evolving landscape of healthcare, the fusion of technology with pharmaceutical and medical sciences has heralded a new era of innovation and progress. This new volume explores the intricate intersections of FDM technology with pharmaceutical and medical realms. It looks at how FDM technology, a 3D printing technique that uses a heated filament to create complex objects layer by ... Read more

    $240.00 USD

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  • Innovations in Drug Manufacturing

    FDM 3D Printing for Pharmaceuticals

    Series series Biomedical and Life Sciences (R0)
    This book offers a comprehensive insight into the application of Fused Deposition Modeling (FDM)—a cutting-edge 3D printing technology—in pharmaceutical manufacturing. As personalized medicine and precision drug delivery gain momentum, FDM emerges as a transformative tool for designing patient-specific dosage forms with enhanced efficiency and control.The book explores the core principles of FDM ... Read more

    $143.09 USD

  • Innovative Pharmaceutical Excipients: Natural Sources

    Series series Biomedical and Life Sciences (R0)
    This book offers an in-depth exploration of the latest advancements in pharmaceutical excipients by addressing the growing need for sustainable and biocompatible options.The book will covers a wide range of topics, including the extraction and characterization of natural polymers, plant-derived excipients, marine polymers, polysaccharides, proteins, peptides, lipids, gums, and mucilages. It ... Read more

    $107.09 USD

  • Precision 3D Printing in Pharmaceutical Sciences

    A Transformative Shift in Drug Manufacturing and Delivery Systems

    Series series Sustainable Computing and Optimization
    This book provides a roadmap for creating customized, precision drug delivery systems and advancing personalized medicine by introducing the revolutionary, transformative role of 3D printing technology in medicine.The convergence of advanced manufacturing techniques with the complexities of pharmaceutical formulation has opened new frontiers of innovation, enabling unprecedented precision in drug ... Read more

    $209.00 USD

  • AI Innovations in Drug Delivery and Pharmaceutical Sciences; Advancing Therapy through Technology

    AI Innovations in Drug Delivery and Pharmaceutical Sciences: Advancing Therapy through Technology offers a comprehensive exploration of how artificial intelligence (AI) is revolutionizing the pharmaceutical and healthcare sectors. This book addresses the AI’s role in drug discovery, development, and delivery, highlighting applications in personalized medicine, nanotechnology, and clinical trials. ... Read more

    $59.00 USD

  • AI Innovations in Drug Delivery and Pharmaceutical Sciences; Advancing Therapy through Technology

    AI Innovations in Drug Delivery and Pharmaceutical Sciences: Advancing Therapy through Technology offers a comprehensive exploration of how artificial intelligence (AI) is revolutionizing the pharmaceutical and healthcare sectors. This book addresses the AI’s role in drug discovery, development, and delivery, highlighting applications in personalized medicine, nanotechnology, and clinical trials. ... Read more

    $42.49 USD

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    Edited by 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 ... Read more

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  • ICH Quality Guidelines

    An Implementation Guide

    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

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  • How to Develop Robust Solid Oral Dosage Forms

    From Conception to Post-Approval

    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

  • New Bioprocessing Strategies: Development and Manufacturing of Recombinant Antibodies and Proteins

    Series Book 165 - Advances in Biochemical Engineering/Biotechnology
    This book review series presents current trends in modern biotechnology. The aim is to cover all aspects of this interdisciplinary technology where knowledge, methods and expertise are required from chemistry, biochemistry, microbiology, genetics, chemical engineering and computer science.Volumes are organized topically and provide a comprehensive discussion of developments in the respective field ... Read more

    $332.09 USD

  • Biopharmaceutical Processing

    Development, Design, and Implementation of Manufacturing Processes

    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 ... Read more

    $332.99 USD

  • Biosimilars Development Strategies

    Fast to Market Approaches

    After 18 years since the first biosimilar was approved, a lot has changed, from the regulatory guidelines to the stakeholder perceptions about the safety and efficacy of biosimilars. However, the development costs remain high, preventing faster entry into markets with more than 200 choices. Analyzing the regulatory filings of all approved biosimilars in the US and EU, a deep analysis of the ... Read more

    $70.99 USD