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  • Regulatory Affairs in the Pharmaceutical Industry

    Edición de Javed Ali, Sanjula Baboota ...
    Regulatory Affairs in the Pharmaceutical Industry is a comprehensive reference that compiles all the information available pertaining to regulatory procedures currently followed by the pharmaceutical industry. Designed to impart advanced knowledge and skills required to learn the various concepts of regulatory affairs, the content covers new drugs, generic drugs and their development, regulatory ... Leer más

    $179.99 USD

  • Nanocarriers for the Delivery of Combination Drugs

    Edición de Sanjula Baboota, Javed Ali ...
    Series series Micro and Nano Technologies
    Nanocarriers for the Delivery of Combination Drugs focuses on the role of nanocarriers in the delivery of combination drugs for the management and treatment of various diseases. Nanocarriers belonging to the category of polymeric nanoparticles, dendrimers, lipidic nanocarriers (like nanoemulsions), liposomes, solid lipid nanoparticles, nanostructured lipid carriers are now being used in the drug ... Leer más

    $197.99 USD

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  • Peptide and Protein Delivery

    Edición de Chris Van Der Walle ...
    The growing area of peptide and protein therapeutics research is of paramount importance to medical application and advancement. A needed reference for entry level researchers and researchers working in interdisciplinary / collaborative projects, Peptide and Protein Delivery addresses the current and emerging routes for delivery of therapeutics. Covering cerebral delivery, pulmonary delivery, ... Leer más

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  • Health Informatics: Practical Guide, Seventh Edition

    Health Informatics: Practical Guide focuses on the application of information technology in healthcare to improve individual and population health, education and research. The goal of the seventh edition is to stimulate and educate healthcare and IT professionals and students about the key topics in this rapidly changing field. Dr. William Hersh from Oregon Health & Science University is the co ... Leer más

    $28.99 USD

  • Natural-Based Polymers for Biomedical Applications

    Series series Woodhead Publishing Series in Biomaterials
    Polymers from natural sources are particularly useful as biomaterials and in regenerative medicine, given their similarity to the extracellular matrix and other polymers in the human body. This important book reviews the wealth of research on both tried and promising new natural-based biomedical polymers, together with their applications as implantable biomaterials, controlled-release carriers or ... Leer más

    $319.99 USD

  • Clinical Research Coordinator Handbook, Fourth Edition

    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, ... Leer más

    $9.99 USD o gratis con Kobo Plus

  • Nanostructures for Oral Medicine

    Series series Nanostructures in Therapeutic Medicine
    Nanostructures for Oral Medicine presents an up-to-date examination of the applications and effects of nanostructured materials in oral medicine, with each chapter addressing recent developments, specific applications, and uses of nanostructures in the oral administration of therapeutic agents in dentistry. The book also includes coverage of the biocompatibility of nanobiomaterials and their ... Leer más

    $175.99 USD

  • Clinical Trials Audit Preparation

    A Guide for Good Clinical Practice (GCP) Inspections

    A must-have guide for any professional in the drug manufacturing industryThe Good Clinical Practice (GCP) audit is a tedious but necessary exercise that assures that all parties do their job properly and in compliance with the applicable FDA code. Clinical Trials Audit Preparation demystifies the audit process for all parties involved, including clinical research sponsors, clinical investigators, ... Leer más

    $97.00 USD

  • Design of Nanostructures for Versatile Therapeutic Applications

    Edición de Alexandru Mihai Grumezescu ...
    Series series Pharmaceutical Nanotechnology
    Design of Nanostructures for Versatile Therapeutic Applications focuses on antimicrobial, antioxidant and nutraceutical applications of nanostructured materials. Many books discuss these subjects, but not from a pharmaceutical point-of-view. This book covers novel approaches related to the modulation of microbial biofilms, antimicrobial therapy and encapsulate polyphenols as antioxidants. Written ... Leer más

    $175.99 USD

  • An Introduction to Pharmacovigilance

    Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problems.This introductory guide is designed to aid the rapid understanding of the key principles of pharmacovigilance. Packed full of examples illustrating drug safety issues it not only covers the processes involved, but the regulatory ... Leer más

    $37.00 USD

  • Chitosan-Based Systems for Biopharmaceuticals

    Delivery, Targeting and Polymer Therapeutics

    Edición de Bruno Sarmento, Jose das Neves ...
    Chitosan is a linear polysaccharide commercially produced by the deacetylation of chitin. It is non-toxic, biodegradable, biocompatible, and acts as a bioadhesive with otherwise unstable biomolecules - making it a valuable component in the formulation of biopharmaceutical drugs.Chitosan-Based Systems for Biopharmaceuticals provides an extensive overview of the application of chitosan and its ... Leer más

    $171.00 USD

  • Pharmacovigilance Medical Writing

    A Good Practice Guide

    Pharmacovigilance Medical Writing covers the preparation of pharmacovigilance documents for all stages of the drug development process (i.e. from clinical development through to applications for marketing authorisations to the post-marketing stage). For each document, the book presents a review of the regulatory framework that governs the content of the document, followed by practical guidance (e ... Leer más

    $51.00 USD