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Books in Pharmaceutical sciences

Elsevier's Pharmaceutical Sciences collection helps pharmaceutical scientists striving to optimize drug design and improve healthcare outcomes by offering comprehensive coverage of every aspect of drug development, integrating disciplines like organic chemistry, biology, and biotechnology. Focused on safety, efficacy, and formulation design, it includes specialized fields such as Clinical Pharmacology and Translational Research, providing valuable insights into the latest advancements in drug discovery.

BooksJournals

    • Mosby's Pharmacy Technician Lab Manual Revised Reprint

      • 1st Edition
      • October 28, 2011
      • Judith Neville
      • English
      • Paperback
        9 7 8 0 3 2 3 0 8 8 1 2 1
      • eBook
        9 7 8 0 3 2 3 2 9 2 6 7 2
      This comprehensive lab manual features more than 49 practical exercises that provide hands-on training for essential pharmacy technician skills. Realistic lab exercises include illustrations of prescription orders, and cover concepts such as hand hygiene, counting medication, prescription interpretation, data entry, pharmacy conversions, inventory management, and prior authorization. Perforated pages make it easy to turn in exercises for evaluation.

    • Clinical Trials

      • 1st Edition
      • October 25, 2011
      • Tom Brody
      • English
      • eBook
        9 7 8 0 1 2 3 9 1 9 1 3 7
      Clinical Trials: Study Design, Endpoints and Biomarkers, Drug Safety, and FDA and ICH Guidelines is a practical guidebook for those engaged in clinical trial design. This book details the organizations and content of clinical trials, including trial design, safety, endpoints, subgroups, HRQoL, consent forms and package inserts. It provides extensive information on both US and international regulatory guidelines and features concrete examples of study design from the medical literature. This book is intended to orient those new to clinical trial design and provide them with a better understanding of how to conduct clinical trials. It will also act as a guide for the more experienced by detailing endpoint selection and illustrating how to avoid unnecessary pitfalls. This book is a straightforward and valuable reference for all those involved in clinical trial design.

    • Pharmacy Management Software for Pharmacy Technicians: A Worktext

      • 2nd Edition
      • September 16, 2011
      • DAA Enterprises, Inc.
      • English
      • eBook
        9 7 8 0 3 2 3 5 8 4 2 3 4
      • eBook
        9 7 8 0 3 2 3 2 6 3 4 6 7
      Gain a head start on your career as a pharmacy technician with Pharmacy Management Software for Pharmacy Technicians, 2nd Edition. This innovative software/worktext package incorporates the full version of real pharmacy management software to give you hands-on training performing the day-to-day tasks of a pharmacy technician just as you will on the job. Easy-to-follow, step-by-step instructions guide you through entering patient data, prescription/medicat... orders, and insurance information, reviewing inventory, and more, enabling you to acquire the skills and experience for professional success before you leave the classroom!

    • An Introduction to Pharmaceutical Sciences

      • 1st Edition
      • July 25, 2011
      • Jiben Roy
      • English
      • Paperback
        9 7 8 1 9 0 7 5 6 8 5 2 7
      • eBook
        9 7 8 1 9 0 8 8 1 8 0 4 1
      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 book makes pharmaceuticals relevant to undergraduate students of pharmacy and pharmaceutical sciences.This book explains how a particular drug was discovered and then converted from lab-scale to manufacturing scale, to the market. It explains the motivation for drug discovery, the reaction chemistry involved, experimental difficulties, various dosage forms and the reasoning behind them, mechanism of action, quality assurance and role of regulatory agencies. After having a course based on this book, the student will be able to understand: 1) the career prospects in the pharmaceutical industry, 2) the need for interdisciplinary teamwork in science, 3) the techniques and technology involved in making pharmaceuticals starting from bulk drugs, and 4) different dosage forms and critical factors in the development of pharmaceutical formulations in relation to the principles of chemistry.A few blockbuster drugs including atorvastatin, sildanefil, ranitidine, ciprofloxacin, amoxicillin, and the longest serving drugs such as aspirin and paracetamol are discussed in detail. Finally, the book also covers the important current pharmaceutical issues like quality control, safety, counterfeiting and abuse of drugs, and future prospects for pharmaceutical industry.

    • Profiles of Drug Substances, Excipients and Related Methodology

      • 1st Edition
      • Volume 36
      • June 16, 2011
      • Harry G. Brittain
      • English
      • Hardback
        9 7 8 0 1 2 3 8 7 6 6 7 6
      • Paperback
        9 7 8 0 3 2 3 1 6 4 4 4 3
      • eBook
        9 7 8 0 1 2 3 8 7 7 0 2 4
      Volumes in this widely revered series present comprehensive reviews of drug substances and additional materials, with critical review chapters that summarize information related to the characterization of drug substances and excipients. This organizational structure meets the needs of the pharmaceutical community and allows for the development of a timely vehicle for publishing review materials on this topic. The scope of the Profiles series encompasses review articles and database compilations that fall within one of the following six broad categories: Physical profiles of drug substances and excipients; Analytical profiles of drug substances and excipients; Drug metabolism and pharmacokinetic profiles of drug substances and excipients; Methodology related to the characterization of drug substances and excipients; Methods of chemical synthesis; and Reviews of the uses and applications for individual drug substances, classes of drug substances, or excipients.

    • Practical Leadership for Biopharmaceutical Executives

      • 1st Edition
      • May 5, 2011
      • Jane Y Chin
      • English
      • Hardback
        9 7 8 1 9 0 7 5 6 8 0 6 0
      • Paperback
        9 7 8 0 0 8 1 0 1 7 3 3 3
      • eBook
        9 7 8 1 9 0 8 8 1 8 0 2 7
      The biohealthcare executive in upper-middle management confronts leadership challenges unique to their industry: they manage highly specialized knowledge workers and innovators, compete at the speed of technology, work in a highly regulated environment where "free speech" often does not apply due to patient safety and privacy concerns, and increasingly are leading virtual teams who may be located in different parts of the world. Practical leadership for biopharmaceutical executives is a guide that strips away the theory and meets head-on the practical leadership challenges these executives face on a daily basis, and provides these "innovator leaders" with the tools to lead effectively in the face of technological complexity.

    • Outsourcing Biopharma R&D to India

      • 1st Edition
      • May 5, 2011
      • P R Chowdhury
      • English
      • Hardback
        9 7 8 1 9 0 7 5 6 8 0 8 4
      • Paperback
        9 7 8 0 0 8 1 0 1 7 3 4 0
      • eBook
        9 7 8 1 9 0 8 8 1 8 0 1 0
      The trend of outsourcing to India for research and development is catching on fast. Over the last decade, worldwide pharmaceutical and biotechnology companies have made India their choice for a research destination. Initially R&D was inclined more towards developing products for the Indian market within the country. This led to several multinational companies opening up production plants in India, primarily due to the globalization of the Indian economy and offshoring jobs to India. Alongside, several global pharma-biotech majors ascertained large market requirements within the country and capitalized on the advantage of serving Indian customers. Strategies were devised to optimize operational expenses with the setting up of on-site R&D to develop products for local requirements. In view of this, this book seeks to explore various nuances of the outsourcing sector with respect to biopharma in India.

    • Cardiovascular Pharmacology: Heart and circulation

      • 1st Edition
      • Volume 59
      • October 21, 2010
      • English
      • Hardback
        9 7 8 0 1 2 3 8 4 9 0 3 8
      • eBook
        9 7 8 0 1 2 3 8 4 9 0 4 5
      Cardiovascular disease remains a major cause of death and disability in developed countries and, increasingly so, in the developing world. Presented in this volume of Advances in Pharmacology are some of the most promising possibilities for treating large numbers of individuals afflicted with these conditions.

    • Progress in Medicinal Chemistry

      • 1st Edition
      • Volume 49
      • October 6, 2010
      • English
      • Paperback
        9 7 8 0 4 4 4 5 6 2 2 5 8
      • Hardback
        9 7 8 0 1 2 3 8 1 2 9 2 6
      • eBook
        9 7 8 0 1 2 3 8 1 2 9 3 3
      Progress in Medicinal Chemistry provides a review of eclectic developments in medicinal chemistry. This volume continues in the serial's tradition of providing an insight into the skills required of the modern medicinal chemist; in particular, the use of an appropriate selection of the wide range of tools now available to solve key scientific problems.

    • Handbook of Modern Pharmaceutical Analysis

      • 2nd Edition
      • Volume 10
      • September 29, 2010
      • Satinder Ahuja + 1 more
      • English
      • Hardback
        9 7 8 0 1 2 3 7 5 6 8 0 0
      • eBook
        9 7 8 0 1 2 3 7 5 9 8 1 8
      Handbook of Modern Pharmaceutical Analysis, Second Edition, synthesizes the complex research and recent changes in the field, while covering the techniques and technology required for today's laboratories. The work integrates strategy, case studies, methodologies, and implications of new regulatory structures, providing complete coverage of quality assurance from the point of discovery to the point of use.

Related subjects

Drug delivery

Drug design

Drug dispensing

Drug manufacturing and packaging

Drug metabolism disposition

Pharmaceutical analysis

Pharmaceutical biotechnology

Pharmaceutical quality control

Pharmaceutical science general

Pharmaceutical technology

Pharmacoeconomics

Pharmacoepidemiology

Pharmacotherapy

Pharmacy

Pharmacy management