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“pp sharma”

Showing 1 - 12 of 12 results for “pp sharma”
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  • Validation in Pharmaceutical Industry

    by P.P. Sharma ...
    The first edition of this book was well received by the pharmaceutical industry and pharmacy education institutions. Over the years, since this book was published, there have been some changes e.g. acceptance limits in media fill trials, acceptance limits in cleaning validation. Thus, there was a need for review of this book.In the first edition, process validation, in general, was discussed and ... Read more

    $100.00 USD or Free with Kobo Plus

  • Stability Studies of Pharmaceutical & Cosmetic Products

    by P.P. Sharma ...
    The purpose of stability testing is to provide evidence on how the quality of an active pharmaceutical ingredient or medicinal product varies with time under the influence of a variety of environmental factors such as temperature, humidity, and light, and to establish a re-test period for the active pharmaceutical ingredient or a shelf life for the medicinal product and recommended storage ... Read more

    $75.00 USD or Free with Kobo Plus

  • Drug Information about Commonly Used Drugs

    by P.P. Sharma ...
    Drug information is something that is needed by all pharma professionals whether in practice, industry, pharmacy education or regulatory. Drug information in this title has been compiled based on their use in disorders of different body systems like gastro-intestinal tract (GIT), respiratory tract, cardio-vascular system. In the introductory section of each part, there is general discussion on ... Read more

    $50.00 USD or Free with Kobo Plus

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  • Process Architecture in Biomanufacturing Facility Design

    Edited by Jeffery Odum, Michael C. Flickinger ...
    Essential information for architects, designers, engineers, equipment suppliers, and other professionals who are working in or entering the biopharmaceutical manufacturing fieldBiomanufacturing facilities that are designed and built today are radically different than in the past. The vital information and knowledge needed to design and construct these increasingly sophisticated biopharmaceutical ... Read more

    $160.00 USD

  • Pharmaceutical Quality by Design

    A Practical Approach

    Edited by Walkiria S. Schlindwein, Mark Gibson ...
    Series series Advances in Pharmaceutical Technology
    A practical guide to Quality by Design for pharmaceutical product developmentPharmaceutical Quality by Design: A Practical Approach outlines a new and proven approach to pharmaceutical product development which is now being rolled out across the pharmaceutical industry internationally. Written by experts in the field, the text explores the QbD approach to product development. This innovative ... Read more

    $90.00 USD

  • Handbook of Validation in Pharmaceutical Processes, Fourth Edition

    Edited by James Agalloco, Phil DeSantis, Anthony Grilli, Anthony Pavell ...
    Revised to reflect significant advances in pharmaceutical production and regulatory expectations, Handbook of Validation in Pharmaceutical Processes, Fourth Edition examines and blueprints every step of the validation process needed to remain compliant and competitive. This book blends the use of theoretical knowledge with recent technological advancements to achieve applied practical solutions. ... Read more

    $69.99 USD

  • ICH Quality Guidelines

    An Implementation Guide

    Edited by 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 ... Read more

    $309.00 USD

  • Cleaning and Cleaning Validation

    A Biotechnology Perspective

    by Jon Voss ...
    This book is intended to serve as a source of practical, technicalinformation for those persons in the biotechnology industry. Casestudies and/ or actual industry examples are used to support the textwherever possible. While much of the material contained within thistext is equally applicable to nonbiopharmaceutical processes, theemphasis has been focused directly upon biopharmaceuticalmanufacturing ... Read more

    $234.99 USD

  • Leachables and Extractables Handbook

    Safety Evaluation, Qualification, and Best Practices Applied to Inhalation Drug Products

    Edited by Douglas J. Ball, Daniel L. Norwood, Cheryl L. M. Stults, Lee M. Nagao ...
    A practical and science-based approach for addressing toxicological concerns related to leachables and extractables associated with inhalation drug productsPackaging and device components of Orally Inhaled and Nasal Drug Products (OINDP)-such as metered dose inhalers, dry powder inhalers, and nasal sprays-pose potential safety risks from leachables and extractables, chemicals that can be released ... Read more

    $129.00 USD

  • Extractables and Leachables

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

    by 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 ... Read more

    $161.00 USD

  • Essential Elements for a GMP Analytical Chemistry Department

    by Thomas Catalano ...
    Series series Biomedical and Life Sciences (R0)
    Essential Elements for a GMP Analytical Chemistry Department is a systematic approach to understanding the essential elements required for a successful GMP Analytical Department to function as an efficient and effective organization. It describes in detail a department structure which allows for the necessary processes to become available to all its personnel in a way where there is a free flow of ... Read more

    $143.09 USD

  • Continuous Manufacturing of Pharmaceuticals

    Edited by Peter Kleinebudde, Johannes Khinast, Jukka Rantanen ...
    Series series Advances in Pharmaceutical Technology
    A comprehensive look at existing technologies and processes for continuous manufacturing of pharmaceuticalsAs rising costs outpace new drug development, the pharmaceutical industry has come under intense pressure to improve the efficiency of its manufacturing processes. Continuous process manufacturing provides a proven solution. Among its many benefits are: minimized waste, energy consumption, ... Read more

    $182.00 USD