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Pharmaceutical technology

Most popular at the top

  • Nanotechnology in Drug Deliveryby Pornanong Aramwit; Glen S. Kwon

    Springer 2008; US$ 269.00

    The reader will be introduced to various aspects of the fundamentals of nanotechnology based drug delivery systems and the application of these systems for the delivery of small molecules, proteins, peptides, oligonucleotides and genes. How these systems overcome challenges offered by biological barriers to drug absorption and drug targeting will also... more...

  • Delivery Technologies for Biopharmaceuticalsby Lene Jorgensen; Hanne Morck Nielson

    Wiley 2009; US$ 207.00

    Advances in biotechnology have provided scientists with an increasing number of biopharmaceuticals such as novel peptide and protein drugs as well as nucleic acid based drugs for gene therapy. However, successful delivery of these biopharmaceuticals is a major challenge because their molecular properties lead to poor physical and chemical stability... more...

  • Cleaning Validation Manualby Syed Imtiaz Haider; Syed Erfan Asif

    CRC Press 2010; US$ 167.95

    CLV-1 How to Establish a Cleaning Validation Program CLV-2 Introduction CLV-3 Scope and Approach CLV-4 Cleaning Validation Team Members and Responsibilities CLV-5 Cleaning Validation Philosophy, Strategies, and Methodology CLV-6 Planning Phase CLV-7 Execution Phase CLV-8 Analytical Testing and Reporting Phase CLV-9 Equipment Description CLV-10... more...

  • Intracellular Deliveryby Ales Prokop

    Springer 2011; US$ 279.00

    This book features a special subsection of Nanomedicine, an application of nanotech nology to achieve breakthroughs in healthcare. It exploits the improved and often novel physical, chemical and biological properties of materials only existent at the nanometer scale. As a consequence of small scale, nanosystems in most cases are efficiently uptaken... more...

  • Management of Chemical and Biological Samples for Screening Applicationsby Mark Wigglesworth; Terry Wood

    Wiley 2012; US$ 200.00

    Filling an obvious gap in the scientific literature, this practice-oriented reference is the first to tie together the working knowledge of large screening centers in the pharmaceutical and biotechnological field. It spans the entire fi eld of this emerging discipline, from compound acquisition to collection optimization for specific purposes, to... more...

  • Drug Deliveryby Monika Schäfer-Korting

    Springer 2010; US$ 489.00

    In the view of most experts pharmacology is on drugs, targets, and actions. In the context the drug as a rule is seen as an active pharmaceutical ingredient and not as a complex mixture of chemical entities of a well defined structure. Today, we are becoming more and more aware of the fact that delivery of the active compound to the target site is... more...

  • Validation of Pharmaceutical Processes, Third Editionby James P. Agalloco; Frederick J. Carleton

    CRC Press 2007; US$ 209.95

    Validation of Pharmaceutical Processes, 3E. Why Validation. Organizing for Validation. Validation and Facility Design. Validation of Environmental Control Systems Used in Parenteral Facilities. Validation of Critical Utilities. The Validation of Pharmaceutical Water Systems. Calibration and Metrology. Temperature Measurements. Qualification... more...

  • New Synthetic Technologies in Medicinal Chemistryby Elizabeth Farrant; David E. Thurston; David Fox

    Royal Society of Chemistry 2011; US$ 160.00

    The modern synthetic chemist applies all the tools available to identify the drug-like molecules with the best chances of becoming novel drugs. This book will act as a primer for graduates and postgraduates interested in a career in drug discovery. It covers both synthetic technologies currently impacting medicinal chemistry and emerging areas. The... more...

  • Good Design Practices for GMP Pharmaceutical Facilitiesby Terry Jacobs; Andrew Signore

    CRC Press 2005; US$ 199.95

    Pharmaceutical Industry Profile. Current Good Manufacturing Practice. Facility Planning. Architecture. Mechanical/HVAC/Utilities. High Purity Water. Automation and Process Controls. Validation and Facility Design. Process Engineering. Oral Solid Dosage Facilities. Sterile Manufacturing Facilities. Biotechnology Facilities. API Facilities.... more...

  • 21 CFR Part 11by Orlando López

    CRC Press 2004; US$ 188.95

    Covering regulatory requirements stipulated by the FDA, this book delineates the organization, planning, verification, and documentation activities and procedural controls required for compliance. The author introduces appropriate supporting technologies such as encryption and digital signatures and places regulatory compliance within the context of... more...